Chimeric fibronectin matrix mimetics and uses thereof

ABSTRACT

The present invention is directed to recombinant fibronectin peptide mimetics and wound healing compositions the same. Other aspects of the present invention include wound healing dressings that comprise the healing composition of the present invention and a wound dressings material and methods of treating wounds using these compositions.

This application is a division of U.S. patent application Ser. No. 13/994,179 which is a national stage application under 35 U.S.C. §371 from PCT International Application No. PCT/US2011/064987, filed Dec. 14, 2011, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/422,923, filed Dec. 14, 2010, which is hereby incorporated by reference in its entirety.

This invention was made with government support under grant number R01GM081513 awarded by the National Institutes of Health. The government has certain rights in this invention.

FIELD OF THE INVENTION

The present invention relates to recombinant fibronectin peptide mimetics and wound healing compositions containing the same. The present invention further relates to methods of treating wounds using the recombinant fibronectin peptide mimetics or compositions of the present invention.

BACKGROUND OF THE INVENTION

Fibronectin is an abundant glycoprotein that is evolutionarily conserved and broadly distributed among vertebrates (Hynes et al., “Fibronectins: Multifunctional Modular Glycoproteins,” J. Cell Biol. 95:369-377 (1982)). Soluble fibronectin is composed of two nearly identical subunits that are joined by disulfide bonds (Petersen et al., “Partial Primary Structure of Bovine Plasma Fibronectin: Three Types of Internal Homology,” Proc. Natl. Acad. Sci. U.S.A. 80:137-141 (1983)). The primary structure of each subunit is organized into three types of repeating homologous units, termed types I, II, and III. Fibronectin type III repeats are found in a number of extracellular matrix (ECM) proteins and consist of two overlapping β sheets (Bork et al., “Proposed Acquisition of an Animal Protein Domain by Bacteria,” Proc. Natl. Acad. Sci. U.S.A. 89(19):8990-8994 (1992) and Leahy et al., “Structure of a Fibronectin Type III Domain From Tenascin Phased by MAD Analysis of the Selenomethionyl Protein,” Science 258:987-991 (1992)). Molecular modeling and atomic force microscopy studies predict that reversible unfolding of the type III repeats contributes to the remarkable elasticity of fibronectin, which may be extended up to six times its initial length without denaturation (Erickson, “Reversible Unfolding of Fibronectin Type III and Immunoglobulin Domains Provides the Structural Basis for Stretch and Elasticity of Titin and Fibronectin,” Proc. Natl. Acad. Sci. 91:10114-10118 (1994) and Oberhauser et al., “The Mechanical Hierarchies of Fibronectin Observed with Single-Molecule AFM,” J. Mol. Biol. 319(2):433-447 (2002)). In the ECM, fibronectin is organized as an extensive network of elongated, branching fibrils. The three-dimensional organization of ECM fibronectin likely arises from the ability of cells to repeatedly exert a mechanical force (Balaban et al., “Force and Focal Adhesion Assembly: A Close Relationship Studied Using Elastic Micropatterned Substrates,” Nat. Cell Biol. 3(5):466-472 (2001)) on discrete regions of the protein (Erickson, “Reversible Unfolding of Fibronectin Type III and Immunoglobulin Domains Provides the Structural Basis for Stretch and Elasticity of Titin and Fibronectin,” Proc. Natl. Acad. Sci. 91:10114-10118 (1994)) to facilitate the formation of fibronectin-fibronectin interactions (Mao et al., “Fibronectin FibrilloGenesis, a Cell-Mediated Matrix Assembly Process,” Matrix Biol. 24(6):389-399 (2005)). As cells contact fibronectin fibrils, tractional forces induce additional conformational changes (Baneyx et al., “Coexisting Conformations of Fibronectin in Cell Culture Imaged Using Fluorescence Resonance Energy Transfer,” Proc. Natl. Acad. Sci. U.S.A. 98(25):14464-14468 (2001)) that are necessary for both lateral growth and branching of the fibrils (Bultmann et al., “Fibronectin Fibrillogenesis Involves the Heparin II Binding Domain of Fibronectin,” J. Biol. Chem. 273:2601-2609 (1998)).

The polymerization of fibronectin into the ECM is a cell-dependent process that is mediated by coordinated events involving the actin cytoskeleton and integrin receptors (Mao et al., “Fibronectin FibrilloGenesis, a Cell-Mediated Matrix Assembly Process,” Matrix Biol. 24(6):389-399 (2005) and Magnusson et al., “Fibronectin: Structure, Assembly, and Cardiovascular Implications,” Arterio. Thromb. Vasc. Biol. 18:1363-1370 (1998)). Most adherent cells, including epithelial cells, endothelial cells, fibroblasts, and smooth muscle cells, polymerize a fibrillar fibronectin matrix (Hynes et al., “Fibronectins: Multifunctional Modular Glycoproteins,” J. Cell Biol. 95:369-377 (1982)). Recent studies have provided evidence that the interaction of cells with either the soluble or ECM form of fibronectin gives rise to distinct cellular phenotypes (Morla et al., “Superfibronectin is a Functionally Distinct Form of Fibronectin,” Nature 367:193-196 (1994) and Hocking et al., “Stimulation of Integrin-Mediated Cell Contractility by Fibronectin Polymerization,” J. Biol. Chem. 275:10673-10682 (2000)). ECM fibronectin stimulates cell spreading (Gui et al., “Identification of the Heparin-Binding Determinants Within Fibronectin Repeat III1: Role in Cell Spreading and Growth,” J. Biol. Chem. 281(46):34816-34825 (2006)), growth (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998) and Sottile et al., “Fibronectin Matrix Assembly Stimulates Cell Growth by RGD-Dependent and -Independent Mechanisms,” J. Cell Sci. 113:4287-4299 (2000)) and migration (Hocking et al., “Fibronectin Polymerization Regulates Small Airway Epithelial Cell Migration,” Am. J. Physiol. Lung Cell Mol. Physiol. 285:L169-L179 (2003)), as well as collagen deposition (Sottile et al., “Fibronectin Polymerization Regulates the Composition and Stability of Extracellular Matrix Fibrils and Cell-Matrix Adhesions,” Mol. Biol. Cell 13:3546-3559 (2002) and Yelling et al., “Polymerization of Type I and III Collagens is Dependent on Fibronectin and Enhanced by Integrins Alpha 11beta 1 and Alpha 2beta 1,” J. Biol. Chem. 277(40):37377-37381 (2002)) and organization (Hocking et al., “Stimulation of Integrin-Mediated Cell Contractility by Fibronectin Polymerization,” J. Biol. Chem. 275:10673-10682 (2000)). Others have shown a role for fibronectin matrix assembly in the deposition of fibrinogen (Pereira et al., “The Incorporation of Fibrinogen Into Extracellular Matrix is Dependent on Active Assembly of a Fibronectin Matrix,” J. Cell Sci. 115(Pt 3):609-617 (2002)), fibrillin (Sabatier et al., “Fibrillin Assembly Requires Fibronectin,” Mol. Biol. Cell 20(3):846-858 (2009)), and tenascin C (Chung et al., “Binding of Tenascin-C to Soluble Fibronectin and Matrix Fibrils,” J. Biol. Chem. 270:29012-29017 (1995)) into the ECM. Fibronectin matrix polymerization stimulates the formation of endothelial ‘neovessels’ in collagen lattices (Zhou et al., “Fibronectin Fibrillogenesis Regulates Three-Dimensional Neovessel Formation,” Genes. Dev. 22(9):1231-1243 (2008)). Moreover, blocking fibronectin matrix polymerization inhibits cell growth (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998) and Mercurius et al., “Inhibition of Vascular Smooth Muscle Growth by Inhibition of Fibronectin Matrix Assembly,” Circ. Res. 82:548-556 (1998)) and contractility (Hocking et al., “Stimulation of Integrin-Mediated Cell Contractility by Fibronectin Polymerization,” J. Biol. Chem. 275:10673-10682 (2000)), alters actin organization (Hocking et al., “Inhibition of Fibronectin Matrix Assembly by the Heparin-Binding Domain of Vitronectin,” J. Biol. Chem. 274:27257-27264 (1999)) and cell signaling (Bourdoulous et al., “Fibronectin Matrix Regulates Activation of RHO and CDC42 GTPases and Cell Cycle Progression,” J. Cell Biol. 143:267-276 (1998)), and inhibits cell migration (Hocking et al., “Fibronectin Polymerization Regulates Small Airway Epithelial Cell Migration,” Am. J. Physiol. Lung Cell Mol. Physiol. 285:L169-L179 (2003)). Together, these studies indicate that fibronectin matrix polymerization plays a key role in establishing the biologically-active extracellular environment required for proper tissue function.

Fibronectin matrix assembly is rapidly up-regulated following tissue injury, while reduced fibronectin matrix deposition is associated with abnormal wound repair (Hynes R O, FIBRONECTINS, (Springer-Verlag 1990)). Altered fibronectin matrix deposition is also associated with a large number of chronic diseases including asthma, liver cirrhosis, and atheroscelerosis (Hynes R O, FIBRONECTINS, (Springer-Verlag 1990); Roberts C R, “Is Asthma a Fibrotic Disease?” Chest 107:111S-117S (1995); and Stenman et al., “Fibronectin and Atherosclerosis,” Acta. Medica. Scandinavia (Supplement) 642:165-170 (1980)). Given the role of the fibronectin matrix in orchestrating ECM organization and in regulating cell and tissue responses critical for tissue repair, defective or diminished fibronectin matrix deposition by cells is likely to have profound effects on the ability of tissues to heal.

The present invention is directed to overcoming these and other deficiencies in the art.

SUMMARY OF THE INVENTION

A first aspect of the present invention is directed to a recombinant fibronectin peptide mimetic that comprises (i) at least a portion of the type III heparin-binding domain FNIII1H of fibronectin, where the portion comprises a heparin binding sequence, and (ii) at least a portion of the type III integrin-binding domain FNIII8-10 of fibronectin, where the portion comprises an integrin binding sequence and wherein the portion does not contain FNIII9 in its entirety.

Other aspects of the present invention are directed to wound healing compositions that comprise the recombinant fibronectin peptide mimetic of the present invention and a synthetic material, and wound healing dressings that comprise the wound healing composition of the present invention and a wound dressing material.

Another aspect of the present invention is directed to a method of treating a wound that involves providing a recombinant fibronectin peptide mimetic or a wound healing composition of the present invention, and applying the peptide mimetic or the composition to the wound under conditions effective to promote healing of the wound.

Several collagen-based dermal substitutes and lyophilized powders derived from porcine, bovine, or human skin are available for wound healing, and a synthetic matrix composed of RGD peptides and hyaluronic acid has shown promise in treating second-degree burn wounds. However, none of these compositions augment extracellular matrix fibronectin function. Described herein is the development of soluble, recombinant fibronectin matrix mimetics that rapidly stimulate cell spreading, migration, and growth upon topical application to tissues in vivo. The use of engineered fibronectin matrix analogs to jump-start′ extracellular matrix fibronectin-mediated cell responses represents a new approach to enhancing cell and tissue function in chronic wounds. Recombinant fibronectin mimetics have several advantages over plasma fibronectin. Firstly, these recombinant mimetics do not require conversion into an “active” form like plasma fibronectin. Secondly, as small molecules, the mimetics are more likely to reach deeper into the wound than the full-length fibronectin. Third, the recombinant mimetics have fewer binding sites for interactions with other molecules, including proteases. Finally, the mimetics are not derived from human blood products, and as recombinant proteins, they are far easier and less expensive to produce on a large scale, and can be assured to be free of infective agents that can be transmitted via blood products.

The soluble recombinant fibronectin mimetics of the present invention are suitable additives to wound healing dressings, creams, hydrogels, etc. that will rapidly stimulate cell function and up-regulate tissue mechanics in tissue wounds, particularly, chronic, non-healing wounds and in damaged tissues. Addition of the fibronectin matrix mimetics to bioengineered scaffolds will enhance the cellular and mechanical properties of dermal substitutes for use with deep wounds and large surface burns. The use of the fibronectin matrix mimetics to promote proper extracellular matrix organization in burns may also reduce contractures and hypertrophic scars that can develop at these sites.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1B show several illustrative fibronectin fusion proteins of the present invention. FIG. 1A is a schematic representation of a fibronectin subunit and recombinant fibronectin fusion proteins. Relevant type III modules are numbered. GST represents the glutathione s-transferase tag used for peptide purification purposes. FNIII1H (1H) represent the heparin-binding, C-terminal fragment of FNIII1; FNIII8 (8), FNIII9 (9), and FNIII10 (10) represent the 8^(th), 9^(th), and 10^(th) fibronectin type III binding domains; and ED_(B)-C (or EDB) represents the corresponding C-terminal fragment of Extra domain-B. In FIG. 1B, aliquots (5 μg) of recombinant proteins were electrophoresed on a 10% SDS-polyacrylamide gel and stained with Coomassie Blue. Numbered lanes correspond to fusion protein identification numbers in FIG. 1A. Molecular mass markers are shown on left.

FIGS. 2A-2B show that GST/III1H,8-10 exhibits greater growth-promoting activity than fibronectin. FN-null MEFs were seeded on tissue culture plates (2.5×10³ cells/cm²) precoated with either 200 nM (FIG. 2A) or increasing concentrations of the various proteins (FIG. 2B) and incubated for 4 days (96 h). FIG. 2A is a panel of phase contrast images that were obtained at 24 h (top row) and 96 h (bottom row). Bar=100 μm. FIG. 2B is a chart quantifying cell number at 96 h as described in the Examples. Data are presented as mean absorbance of quadruplicate wells±SEM and represent 1 of 3 experiments. *Significantly greater than FN, p<0.05 (ANOVA).

FIGS. 3A-3B depict the analyses of protein surface adsorption and cell adhesion. Tissue culture plates were coated with increasing concentrations of the indicated fibronectin peptide mimetics. The relative amount of peptide bound to wells was determined by ELISA and shown in the graph of FIG. 3A. In FIG. 3B, FN-null MEFs were seeded onto protein-coated wells (1.5×10⁵ cells/cm²) and allowed to attach for 30 min. The number of adherent cells was determined as described infra in the Examples. Data are presented as mean absorbance of triplicate wells±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 4A-4D demonstrate that FNIII1H is essential for the enhanced growth response. FN-null MEFs were seeded at a density of 2.5×10³ cells/cm² (FIGS. 4A and 4C) or 1.5×10⁵ cells/cm² (FIGS. 4B and 4D) on tissue culture plates coated with 200 nM recombinant fibronectin constructs. In FIGS. 4A and 4C, relative cell number was determined after 4 days. In FIGS. 4B and 4D, cells were allowed to adhere for 30 min and attached cell number was determined. Data are expressed as mean absorbance of quadruplicate wells±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 5A-5B show that FNIII8 and FNIII10 are required for cell growth responses. FN-null MEFs were seeded at a density of 2.5×10³ cells/cm² (FIG. 5A) or 1.5×10⁵ cells/cm² (FIG. 5B) onto tissue culture plates precoated with 200 nM of the recombinant fibronectin constructs. In FIG. 5A, relative cell number was determined after 4 days. In FIG. 5B, cells were allowed to adhere for 30 min and the number of attached cells was determined. Data are expressed as mean absorbance of quadruplicate wells±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 6A-6B show that the chimeric matrix mimetics of the present invention support cell adhesion and growth. FN-null MEFs were seeded at 1.5×10⁵ cells/cm² (FIG. 6A) or 2.5×10³ cells/cm² (FIG. 6B) on tissue culture plates coated with protein at increasing concentrations (FIG. 6A) or at 200 nM (FIG. 6B). GRGDSP (SEQ ID NO: 24) peptides were coated at 20 μg/ml (34 mM). In FIG. 6A, cells were allowed to adhere for 30 min and attached cell number was determined. In FIG. 6B, relative cell number was determined after 4 days. Data are expressed as mean absorbance of triplicate wells (FIG. 6A) or quadruplicate wells (FIG. 6B)±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 7A-7B depict a role of FNIII1H in the proliferative response to GST/III1H,8^(RGD). FN-null MEFs were seeded at a density of 2.5×10³ cells/cm² (FIG. 7A) or 1.5×10⁵ cells/cm² (FIG. 7B) on tissue culture plates coated with recombinant fibronectin constructs at increasing concentrations (FIG. 7A) or 400 nM (FIG. 7B). Relative cell number was determined after 4 days (FIG. 7A) or cells were allowed to adhere for 30 min and attached cell number was determined (FIG. 7B). Data are expressed as mean absorbance of quadruplicate wells±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIG. 8 shows the proliferative response to fibronectin matrix mimetics of the present invention compared to other ECM proteins. FN-null MEFs were seeded (2.5×10³ cells/cm²) on tissue culture plates coated with various proteins at a concentration of 200 nM. Relative cell number was determined after 4 days. Data are expressed as mean absorbance of quadruplicate wells±SEM and represent 1 of 3 experiments. *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 9A-9C demonstrate that fibronectin matrix mimetics support cell migration. FN-null MEFs were seeded (7.4×10⁴ cells/cm²) on tissue culture plates coated with 200 nM plasma fibronectin (FN) or the various indicated recombinant fibronectin constructs. Cells were allowed to spread to confluence for 16 h (FIGS. 9A and 9B) or 4 h (FIG. 9C). Cell monolayers were wounded and images of five non-overlapping regions were obtained at 0, 2, 4, 6, and 8 hours post-wounding. Data are presented as mean area migrated at each time point±SEM and represent 1 of 3 experiments. In FIGS. 9A and 9B, * significantly different from FN, p<0.05. In FIG. 9C, * significantly different from GST/III1H,8,10, p<0.05 (ANOVA).

FIG. 10 shows that fibronectin matrix mimetics of the present invention stimulate collagen gel contraction. FN-null MEFs were imbedded (2×10⁵ cells/ml) in neutralized collagen gels in the presence of recombinant fibronectin constructs, the control protein, GST (400 nM), or plasma fibronectin (20 mg/ml; 40 nM). Collagen gel contraction was determined after 20 h as described infra in the Examples. Data are presented as average percent contraction versus ‘no-cell’ controls from 3 experiments performed in quadruplicate±SEM. * Significantly different from GST, p<0.05. ^(#)Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 11A-11D show the selective integrin-mediated adhesion to fibronectin matrix mimetics. FN-null MEFs were seeded onto tissue culture plates pre-coated with 400 nM GST/III1H,8-10 (FIG. 11A), GST/III1H,8,10 (FIG. 11B), GST/III1H,8RGD (FIG. 11C), or 10 nM full-length fibronectin (FIG. 11D), in the presence of integrin function-blocking antibodies, isotype-matched control antibodies (+IgG+IgM), or EDTA. Cell adhesion was determined as described infra in the Examples. Data are compiled from 3 separate experiments each performed in triplicate. Values are represented as mean fold difference from ‘+IgG+IgM’ control+/−SEM. *Significantly different from ‘+IgG+IgM’, p<0.05 (ANOVA).

FIG. 12 shows that αvβ3-binding substrates support fibronectin matrix assembly. FN-null MEFs were seeded (3.0×10⁴ cells/cm²) onto tissue culture plates pre-coated with matrix mimetics (400 nM) or fibronectin (10 nM). Four hours after seeding, fibronectin (10 μg/ml) was added to each well, and cells were incubated for an additional 20 h. Cells were processed for immunofluorescence microscopy as described infra. Fibronectin fibrils were visualized using a polyclonal anti-fibronectin antibody. Actin was visualized using Alexa⁴⁸⁸ labeled phalloidin. Images represent 1 of 3 experiments. Bar=10 μm.

FIGS. 13A-13C show the quantification of fibronectin matrix accumulation. FN-null MEFs were seeded (3.0×10⁴ cells/cm²) on tissue culture plates pre-coated with matrix mimetics at 400 nM. Four hours after seeding, unlabeled (FIGS. 13A and 13B) or Alexa⁴⁸⁸-labeled (FIG. 13C) fibronectin was added at 10 μg/ml and cells were incubated for 20 h. FIG. 13A is an immunoblot analysis of whole cell lysates using antibodies directed against fibronectin and α-tubulin. Immunoblot represents 1 of 3 experiments each performed in duplicate wells. Fibronectin band intensities of immunoblots were quantified by densitometry and the results are shown in the graph of FIG. 13B. *Significantly different from GST/III1H,8-10, p<0.05. ^(#)Significantly greater than GST/III1H,8,10, p<0.05 (ANOVA). In FIG. 13C, Alexa⁴⁸⁸-fibronectin accumulation was determined. Data are presented as mean fluorescence+/−SEM and represent 1 of 3 experiments. * Significantly different from GST/III1H,8-10, p<0.05. #Significantly greater than GST/III1H,8,10, p<0.05 (ANOVA).

FIGS. 14A-14C show collagen I deposition by cells adherent to matrix mimetics. FN-null MEFs were seeded (3.0×10⁴ cells/cm²) on tissue culture plates pre-coated with matrix mimetics (400 nM). Four hours after seeding, cells were treated with fibronectin (10 μg/ml) and FITC-collagen I (10 μg/ml) for 20 h. In FIG. 14A, control wells received either FITC-collagen I only (+cell, −FN) or FITC collagen I in the absence of both cells and fibronectin (−cells, −FN). FITC-collagen I binding was quantified and data are presented as mean fluorescence intensity+/−SEM and represent 1 of 3 experiments performed in quadruplicate. *Significantly different from GST/III1H,8-10, p<0.05. # Significantly greater than GST/III1H,8,10, p<0.05 (ANOVA). In FIG. 14B, cells were processed for immunofluorescence microscopy and stained using an antibody against fibronectin. Images represent 1 of 3 experiments. Bar=10 μm. Four hours after seeding, cells were treated with fibronectin (10 μg/ml) and FITC-collagen I (10 μm/ml) in the presence of either R1R2 (250 nM) or FNIII11C (250 nM). FITC-collagen I was quantified after 20 h and the results are shown in FIG. 14C. Data are presented as mean fluorescence+/−SEM and represent 1 of 3 experiments performed in quadruplicate. * Significantly different from III11C treatment, p<0.05 (ANOVA).

FIG. 15 shows α5β1 integrin translocation on αvβ3-binding substrates. FN-null MEFs were seeded (3.0×10⁴ cells/cm²) on tissue culture plates pre-coated with fibronectin matrix mimetics (400 nM) or full-length fibronectin (10 nM). Four hours after seeding, soluble fibronectin (10m/ml) was added to each well and cells were incubated for 20 h. Cells were processed for immunofluorescence microscopy and stained using antibodies directed against fibronectin and α5 integrin. Images represent 1 of 3 experiments. Bar=10 μm.

FIGS. 16A-16C show substrate-dependent ligation and clustering of α5β1 integrins. FN-null MEFs were seeded at a density of 2.5×10³ cells/cm² (FIG. 16A) or 3×10⁴ cells/cm² (FIG. 16B) onto tissue culture plates precoated with 400 nM of the various fibronectin matrix mimetics or 10 nM full-length fibronectin and allowed to adhere and spread for 4 h. In FIG. 16A, cells were processed for immunofluorescence microscopy and stained using antibodies against α5 integrin and vinculin. Images represent 1 of 3 experiments. Bar=10 μm. In FIG. 16B, cell surface proteins bound to the adhesive substrates were cross-linked using bis(sulfosuccinimidyl)suberate (BS³). Unbound proteins were extracted and cross-linked. α5 integrins were analyzed by immunoblotting. Immunoblot represents 1 of 3 experiments each performed in duplicate wells. α5 integrin band intensities of immunoblots were quantified and compiled from 3 separate experiments each performed in duplicate wells (FIG. 16C). *Significantly different from GST/III1H,8-10, p<0.05 (ANOVA).

FIGS. 17A-17C show that the coating density of GST/III1H,8-10 controls fibronectin matrix assembly. FN-null MEFs were seeded (3.0×10⁴ cells/cm²) onto tissue culture plates pre-coated with GST/III1H,8-10 at indicated concentrations. Four hours after seeding, cell surface proteins bound to the mimetic adhesive substrate were cross-linked using BS³. Cells were extracted and ligated cell surface proteins were analyzed by immunoblotting with an anti-α5 integrin antibody (FIG. 17A). Immunoblot represents 1 of 3 experiments each performed in duplicate wells. α5 integrin band intensities were quantified and compiled from 3 separate experiments each performed in duplicate wells (FIG. 17B). *Significantly different from 400 nM GST/III1H,8-10, p<0.05 (ANOVA). Four hours after seeding, fibronectin (10 m/ml) was added and cells were incubated an additional 20 h. Cells were processed for immunofluorescence microscopy and stained using antibodies against fibronectin and α5 integrin (FIG. 17C). Images represent 1 of 3 experiments. Bar=10 μm.

FIGS. 18A-18B show fibronectin-stimulated cell proliferation on matrix-supporting substrates. FN-null MEFs were seeded at a density of 2.5×10³ cells/cm² (FIG. 18A) or 3.0×10⁴ cells/cm² (FIG. 18B) on tissue culture plates pre-coated with matrix mimetics (50 nM) or collagen I (50 μg/ml). Four hours after seeding, fibronectin (10 μg/ml) or an equal volume of PBS was added and cells were incubated for 4 d. Cell number was determined and is shown FIG. 18A. The data are expressed as mean absorbance of triplicate wells+/−SEM and represent 1 of 3 experiments. *Significantly different from +PBS treatment, p<0.05 (ANOVA). In FIG. 18B, four hours after seeding, Alexa⁴⁸⁸-labeled fibronectin (FN488; 10 μg/ml) was added to cells and incubated an additional 20 h. FN488 accumulation was quantified. Some wells received FN488 in the absence of cells (−cells) to assess fibronectin-substrate binding. Data are presented as mean fluorescence of quadruplicate wells+/−SEM and represent 1 of 3 experiments. *Significantly greater than all other substrates, p<0.05 (ANOVA).

FIGS. 19A-19B show that GST/III1H,8,10 and GST/III1H,8RGD increase granulation tissue thickness in diabetic mice. Full thickness skin wounds were made on the dorsal side of C57BLKS/J-m+/+Lepr(db) mice (age 8-12 weeks) using a 6 mm biopsy punch (Miltex). Wounds were treated with either 15 μl of either mimetic or GST (25 μM diluted in PBS) or PBS alone. Wounds were sealed from the environment with a 1 cm×1 cm piece of Tegaderm™ (3M Health Care). Mice were treated with mimetics immediately following surgery as well as on days 2, 4, 7, 9, 11, 14 and 16 after surgery with new Tegaderm™ being applied following each treatment. Fourteen days (n=3) or 18 days (n=1) after wounding, the animals were sacrificed and the skin surrounding the wound was excised (FIG. 19A, inset images) and embedded in paraffin. Four-micrometer sections were cut, mounted on slides, and stained for hematoxylin and eosin. Slides were viewed using an inverted microscope (Carl Zeiss MicroImaging) with a 5× objective. Images of the wound space were obtained with a digital camera (Model Infinity 2; Lumenera) and represent 1 of 4 experiments (FIG. 19A). Bar=200 μm. FIG. 19B is a graph showing mean granulation tissue thickness quantified for 3 separate hematoxylin and eosin stained slides per mouse. Granulation tissue thickness was defined as the distance from the bottom of the epidermis to the top of the subcutaneous fat layer. Data are compiled from 4 separate experiments and are presented as the mean granulation tissue thickness+/−SEM. *Significantly different from GST, p<0.05 (ANOVA). ^(#)Significantly different from PBS, p<0.05 (ANOVA).

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates generally to recombinant fibronectin matrix mimetics, wound healing compositions containing the recombinant mimetics, and their use in promoting wound healing and tissue regneration.

A first aspect of the present invention relates to a recombinant fibronectin peptide mimetic that comprises (i) at least a portion of the type III heparin-binding domain FNIII1H of fibronectin, where the portion comprises a heparin binding sequence, and (ii) at least a portion of the type III integrin-binding domain FNIII8-10 of fibronectin, where the portion comprises an integrin binding sequence and wherein the portion does not contain FNIII9 in its entirety. As described herein, nucleic acid molecules encoding the recombinant fibronectin peptide mimetic of the present invention and expression vectors comprising these nucleic acid molecules are also encompassed by the present invention.

Soluble fibronectin is composed of two nearly identical subunits that are joined by disulfide bonds. FIG. 1A shows a schematic representation of a fibronectin subunit. As shown, the primary structure of each subunit is organized into three types of repeating homologous units, termed types I, II, and III. The relevant type III modules (i.e., type III modules FNIII1, FNIII8, FNIII9, FNIII10, and FNIII13) in FIG. 1A are numbered. The composition of the various recombinant fibronectin peptide mimetics of the present invention are also shown below the schematic of the fibronectin subunit in FIG. 1A (numbered 1-11).

In describing the recombinant fibronectin peptide mimetics of the present invention, reference is made to the full-length human fibronectin amino acid sequence isoform 1 (UniProtKB/Swiss-Prot No. P02751, which is hereby incorporated by reference in its entirety) which is shown below as SEQ ID NO: 1. When describing the construction of the peptide mimetics of the present invention in the Examples, the amino acid residue positions referred to are in reference to the more mature fibronectin protein sequence that does not contain the 31-amino acid leader sequence. One of skill in the art readily appreciates, for example, that the FNIII1H domain comprises amino acid residues 628-704 of SEQ ID NO:1, but comprises amino acid residues 597-673 of the more mature fibronectin protein (i.e., the fibronectin protein without the 31-amino acid leader sequence).

SEQ ID NO: 1 Human Fibronectin Met Leu Arg Gly Pro Gly Pro Gly Leu Leu Leu Leu Ala Val Gln Cys 1               5                   10                  15 Leu Gly Thr Ala Val Pro Ser Thr Gly Ala Ser Lys Ser Lys Arg Gln             20                  25                  30 Ala Gln Gln Met Val Gln Pro Gln Ser Pro Val Ala Val Ser Gln Ser         35                  40                  45 Lys Pro Gly Cys Tyr Asp Asn Gly Lys His Tyr Gln Ile Asn Gln Gln     50                  55                  60 Trp Glu Arg Thr Tyr Leu Gly Asn Ala Leu Val Cys Thr Cys Tyr Gly 65                  70                  75                  80 Gly Ser Arg Gly Phe Asn Cys Glu Ser Lys Pro Glu Ala Glu Glu Thr                 85                  90                  95 Cys Phe Asp Lys Tyr Thr Gly Asn Thr Tyr Arg Val Gly Asp Thr Tyr             100                 105                 110 Glu Arg Pro Lys Asp Ser Met Ile Trp Asp Cys Thr Cys Ile Gly Ala         115                 120                 125 Gly Arg Gly Arg Ile Ser Cys Thr Ile Ala Asn Arg Cys His Glu Gly     130                 135                 140 Gly Gln Ser Tyr Lys Ile Gly Asp Thr Trp Arg Arg Pro His Glu Thr 145                 150                 155                 160 Gly Gly Tyr Met Leu Glu Cys Val Cys Leu Gly Asn Gly Lys Gly Glu                 165                 170                 175 Trp Thr Cys Lys Pro Ile Ala Glu Lys Cys Phe Asp His Ala Ala Gly             180                 185                 190 Thr Ser Tyr Val Val Gly Glu Thr Trp Glu Lys Pro Tyr Gln Gly Trp         195                 200                 205 Met Met Val Asp Cys Thr Cys Leu Gly Glu Gly Ser Gly Arg Ile Thr     210                 215                 220 Cys Thr Ser Arg Asn Arg Cys Asn Asp Gln Asp Thr Arg Thr Ser Tyr 225                 230                 235                 240 Arg Ile Gly Asp Thr Trp Ser Lys Lys Asp Asn Arg Gly Asn Leu Leu                 245                 250                 255 Gln Cys Ile Cys Thr Gly Asn Gly Arg Gly Glu Trp Lys Cys Glu Arg             260                 265                 270 His Thr Ser Val Gln Thr Thr Ser Ser Gly Ser Gly Pro Phe Thr Asp         275                 280                 285 Val Arg Ala Ala Val Tyr Gln Pro Gln Pro His Pro Gln Pro Pro Pro     290                 295                 300 Tyr Gly His Cys Val Thr Asp Ser Gly Val Val Tyr Ser Val Gly Met 305                 310                 315                 320 Gln Trp Leu Lys Thr Gln Gly Asn Lys Gln Met Leu Cys Thr Cys Leu                 325                 330                 335 Gly Asn Gly Val Ser Cys Gln Glu Thr Ala Val Thr Gln Thr Tyr Gly             340                 345                 350 Gly Asn Ser Asn Gly Glu Pro Cys Val Leu Pro Phe Thr Tyr Asn Gly         355                 360                 365 Arg Thr Phe Tyr Ser Cys Thr Thr Glu Gly Arg Gln Asp Gly His Leu     370                 375                 380 Trp Cys Ser Thr Thr Ser Asn Tyr Glu Gln Asp Gln Lys Tyr Ser Phe 385                 390                 395                 400 Cys Thr Asp His Thr Val Leu Val Gln Thr Arg Gly Gly Asn Ser Asn                 405                 410                 415 Gly Ala Leu Cys His Phe Pro Phe Leu Tyr Asn Asn His Asn Tyr Thr             420                 425                 430 Asp Cys Thr Ser Glu Gly Arg Arg Asp Asn Met Lys Trp Cys Gly Thr         435                 440                 445 Thr Gln Asn Tyr Asp Ala Asp Gln Lys Phe Gly Phe Cys Pro Met Ala     450                 455                 460 Ala His Glu Glu Ile Cys Thr Thr Asn Glu Gly Val Met Tyr Arg Ile 465                 470                 475                 480 Gly Asp Gln Trp Asp Lys Gln His Asp Met Gly His Met Met Arg Cys                 485                 490                 495 Thr Cys Val Gly Asn Gly Arg Gly Glu Trp Thr Cys Ile Ala Tyr Ser             500                 505                 510 Gln Leu Arg Asp Gln Cys Ile Val Asp Asp Ile Thr Tyr Asn Val Asn         515                 520                 525 Asp Thr Phe His Lys Arg His Glu Glu Gly His Met Leu Asn Cys Thr     530                 535                 540 Cys Phe Gly Gln Gly Arg Gly Arg Trp Lys Cys Asp Pro Val Asp Gln 545                 550                 555                 560 Cys Gln Asp Ser Glu Thr Gly Thr Phe Tyr Gln Ile Gly Asp Ser Trp                 565                 570                 575 Glu Lys Tyr Val His Gly Val Arg Tyr Gln Cys Tyr Cys Tyr Gly Arg             580                 585                 590 Gly Ile Gly Glu Trp His Cys Gln Pro Leu Gln Thr Tyr Pro Ser Ser         595                 600                 605 Ser Gly Pro Val Glu Val Phe Ile Thr Glu Thr Pro Ser Gln Pro Asn     610                 615                 620 Ser His Pro Ile Gln Trp Asn Ala Pro Gln Pro Ser His Ile Ser Lys 625                 630                 635                 640 Tyr Ile Leu Arg Trp Arg Pro Lys Asn Ser Val Gly Arg Trp Lys Glu                 645                 650                 655 Ala Thr Ile Pro Gly His Leu Asn Ser Tyr Thr Ile Lys Gly Leu Lys             660                 665                 670 Pro Gly Val Val Tyr Glu Gly Gln Leu Ile Ser Ile Gln Gln Tyr Gly         675                 680                 685 His Gln Glu Val Thr Arg Phe Asp Phe Thr Thr Thr Ser Thr Ser Thr     690                 695                 700 Pro Val Thr Ser Asn Thr Val Thr Gly Glu Thr Thr Pro Phe Ser Pro 705                 710                 715                 720 Leu Val Ala Thr Ser Glu Ser Val Thr Glu Ile Thr Ala Ser Ser Phe                 725                 730                 735 Val Val Ser Trp Val Ser Ala Ser Asp Thr Val Ser Gly Phe Arg Val             740                 745                 750 Glu Tyr Glu Leu Ser Glu Glu Gly Asp Glu Pro Gln Tyr Leu Asp Leu         755                 760                 765 Pro Ser Thr Ala Thr Ser Val Asn Ile Pro Asp Leu Leu Pro Gly Arg     770                 775                 780 Lys Tyr Ile Val Asn Val Tyr Gln Ile Ser Glu Asp Gly Glu Gln Ser 785                 790                 795                 800 Leu Ile Leu Ser Thr Ser Gln Thr Thr Ala Pro Asp Ala Pro Pro Asp                 805                 810                 815 Thr Thr Val Asp Gln Val Asp Asp Thr Ser Ile Val Val Arg Trp Ser             820                 825                 830 Arg Pro Gln Ala Pro Ile Thr Gly Tyr Arg Ile Val Tyr Ser Pro Ser         835                 840                 845 Val Glu Gly Ser Ser Thr Glu Leu Asn Leu Pro Glu Thr Ala Asn Ser     850                 855                 860 Val Thr Leu Ser Asp Leu Gln Pro Gly Val Gln Tyr Asn Ile Thr Ile 865                 870                 875                 880 Tyr Ala Val Glu Glu Asn Gln Glu Ser Thr Pro Val Val Ile Gln Gln                 885                 890                 895 Glu Thr Thr Gly Thr Pro Arg Ser Asp Thr Val Pro Ser Pro Arg Asp             900                 905                 910 Leu Gln Phe Val Glu Val Thr Asp Val Lys Val Thr Ile Met Trp Thr         915                 920                 925 Pro Pro Glu Ser Ala Val Thr Gly Tyr Arg Val Asp Val Ile Pro Val     930                 935                 940 Asn Leu Pro Gly Glu His Gly Gln Arg Leu Pro Ile Ser Arg Asn Thr 945                 950                 955                 960 Phe Ala Glu Val Thr Gly Leu Ser Pro Gly Val Thr Tyr Tyr Phe Lys                 965                 970                 975 Val Phe Ala Val Ser His Gly Arg Glu Ser Lys Pro Leu Thr Ala Gln             980                 985                 990 Gln Thr Thr Lys Leu Asp Ala Pro Thr Asn Leu Gln Phe Val Asn Glu         995                 1000                1005 Thr Asp Ser Thr Val Leu Val Arg Trp Thr Pro Pro Arg Ala Gln     1010                1015                1020 Ile Thr Gly Tyr Arg Leu Thr Val Gly Leu Thr Arg Arg Gly Gln     1025                1030                1035 Pro Arg Gln Tyr Asn Val Gly Pro Ser Val Ser Lys Tyr Pro Leu     1040                1045                1050 Arg Asn Leu Gln Pro Ala Ser Glu Tyr Thr Val Ser Leu Val Ala     1055                1060                1065 Ile Lys Gly Asn Gln Glu Ser Pro Lys Ala Thr Gly Val Phe Thr     1070                1075                1080 Thr Leu Gln Pro Gly Ser Ser Ile Pro Pro Tyr Asn Thr Glu Val     1085                1090                1095 Thr Glu Thr Thr Ile Val Ile Thr Trp Thr Pro Ala Pro Arg Ile     1100                1105                1110 Gly Phe Lys Leu Gly Val Arg Pro Ser Gln Gly Gly Glu Ala Pro     1115                1120                1125 Arg Glu Val Thr Ser Asp Ser Gly Ser Ile Val Val Ser Gly Leu     1130                1135                1140 Thr Pro Gly Val Glu Tyr Val Tyr Thr Ile Gln Val Leu Arg Asp     1145                1150                1155 Gly Gln Glu Arg Asp Ala Pro Ile Val Asn Lys Val Val Thr Pro     1160                1165                1170 Leu Ser Pro Pro Thr Asn Leu His Leu Glu Ala Asn Pro Asp Thr     1175                1180                1185 Gly Val Leu Thr Val Ser Trp Glu Arg Ser Thr Thr Pro Asp Ile     1190                1195                1200 Thr Gly Tyr Arg Ile Thr Thr Thr Pro Thr Asn Gly Gln Gln Gly     1205                1210                1215 Asn Ser Leu Glu Glu Val Val His Ala Asp Gln Ser Ser Cys Thr     1220                1225                1230 Phe Asp Asn Leu Ser Pro Gly Leu Glu Tyr Asn Val Ser Val Tyr     1235                1240                1245 Thr Val Lys Asp Asp Lys Glu Ser Val Pro Ile Ser Asp Thr Ile     1250                1255                1260 Ile Pro Ala Val Pro Pro Pro Thr Asp Leu Arg Phe Thr Asn Ile     1265                1270                1275 Gly Pro Asp Thr Met Arg Val Thr Trp Ala Pro Pro Pro Ser Ile     1280                1285                1290 Asp Leu Thr Asn Phe Leu Val Arg Tyr Ser Pro Val Lys Asn Glu     1295                1300                1305 Glu Asp Val Ala Glu Leu Ser Ile Ser Pro Ser Asp Asn Ala Val     1310                1315                1320 Val Leu Thr Asn Leu Leu Pro Gly Thr Glu Tyr Val Val Ser Val     1325                1330                1335 Ser Ser Val Tyr Glu Gln His Glu Ser Thr Pro Leu Arg Gly Arg     1340                1345                1350 Gln Lys Thr Gly Leu Asp Ser Pro Thr Gly Ile Asp Phe Ser Asp     1355                1360                1365 Ile Thr Ala Asn Ser Phe Thr Val His Trp Ile Ala Pro Arg Ala     1370                1375                1380 Thr Ile Thr Gly Tyr Arg Ile Arg His His Pro Glu His Phe Ser     1385                1390                1395 Gly Arg Pro Arg Glu Asp Arg Val Pro His Ser Arg Asn Ser Ile     1400                1405                1410 Thr Leu Thr Asn Leu Thr Pro Gly Thr Glu Tyr Val Val Ser Ile     1415                1420                1425 Val Ala Leu Asn Gly Arg Glu Glu Ser Pro Leu Leu Ile Gly Gln     1430                1435                1440 Gln Ser Thr Val Ser Asp Val Pro Arg Asp Leu Glu Val Val Ala     1445                1450                1455 Ala Thr Pro Thr Ser Leu Leu Ile Ser Trp Asp Ala Pro Ala Val     1460                1465                1470 Thr Val Arg Tyr Tyr Arg Ile Thr Tyr Gly Glu Thr Gly Gly Asn     1475                1480                1485 Ser Pro Val Gln Glu Phe Thr Val Pro Gly Ser Lys Ser Thr Ala     1490                1495                1500 Thr Ile Ser Gly Leu Lys Pro Gly Val Asp Tyr Thr Ile Thr Val     1505                1510                1515 Tyr Ala Val Thr Gly Arg Gly Asp Ser Pro Ala Ser Ser Lys Pro     1520                1525                1530 Ile Ser Ile Asn Tyr Arg Thr Glu Ile Asp Lys Pro Ser Gln Met     1535                1540                1545 Gln Val Thr Asp Val Gln Asp Asn Ser Ile Ser Val Lys Trp Leu     1550                1555                1560 Pro Ser Ser Ser Pro Val Thr Gly Tyr Arg Val Thr Thr Thr Pro     1565                1570                1575 Lys Asn Gly Pro Gly Pro Thr Lys Thr Lys Thr Ala Gly Pro Asp     1580                1585                1590 Gln Thr Glu Met Thr Ile Glu Gly Leu Gln Pro Thr Val Glu Tyr     1595                1600                1605 Val Val Ser Val Tyr Ala Gln Asn Pro Ser Gly Glu Ser Gln Pro     1610                1615                1620 Leu Val Gln Thr Ala Val Thr Asn Ile Asp Arg Pro Lys Gly Leu     1625                1630                1635 Ala Phe Thr Asp Val Asp Val Asp Ser Ile Lys Ile Ala Trp Glu     1640                1645                1650 Ser Pro Gln Gly Gln Val Ser Arg Tyr Arg Val Thr Tyr Ser Ser     1655                1660                1665 Pro Glu Asp Gly Ile His Glu Leu Phe Pro Ala Pro Asp Gly Glu     1670                1675                1680 Glu Asp Thr Ala Glu Leu Gln Gly Leu Arg Pro Gly Ser Glu Tyr     1685                1690                1695 Thr Val Ser Val Val Ala Leu His Asp Asp Met Glu Ser Gln Pro     1700                1705                1710 Leu Ile Gly Thr Gln Ser Thr Ala Ile Pro Ala Pro Thr Asp Leu     1715                1720                1725 Lys Phe Thr Gln Val Thr Pro Thr Ser Leu Ser Ala Gln Trp Thr     1730                1735                1740 Pro Pro Asn Val Gln Leu Thr Gly Tyr Arg Val Arg Val Thr Pro     1745                1750                1755 Lys Glu Lys Thr Gly Pro Met Lys Glu Ile Asn Leu Ala Pro Asp     1760                1765                1770 Ser Ser Ser Val Val Val Ser Gly Leu Met Val Ala Thr Lys Tyr     1775                1780                1785 Glu Val Ser Val Tyr Ala Leu Lys Asp Thr Leu Thr Ser Arg Pro     1790                1795                1800 Ala Gln Gly Val Val Thr Thr Leu Glu Asn Val Ser Pro Pro Arg     1805                1810                1815 Arg Ala Arg Val Thr Asp Ala Thr Glu Thr Thr Ile Thr Ile Ser     1820                1825                1830 Trp Arg Thr Lys Thr Glu Thr Ile Thr Gly Phe Gln Val Asp Ala     1835                1840                1845 Val Pro Ala Asn Gly Gln Thr Pro Ile Gln Arg Thr Ile Lys Pro     1850                1855                1860 Asp Val Arg Ser Tyr Thr Ile Thr Gly Leu Gln Pro Gly Thr Asp     1865                1870                1875 Tyr Lys Ile Tyr Leu Tyr Thr Leu Asn Asp Asn Ala Arg Ser Ser     1880                1885                1890 Pro Val Val Ile Asp Ala Ser Thr Ala Ile Asp Ala Pro Ser Asn     1895                1900                1905 Leu Arg Phe Leu Ala Thr Thr Pro Asn Ser Leu Leu Val Ser Trp     1910                1915                1920 Gln Pro Pro Arg Ala Arg Ile Thr Gly Tyr Ile Ile Lys Tyr Glu     1925                1930                1935 Lys Pro Gly Ser Pro Pro Arg Glu Val Val Pro Arg Pro Arg Pro     1940                1945                1950 Gly Val Thr Glu Ala Thr Ile Thr Gly Leu Glu Pro Gly Thr Glu     1955                1960                1965 Tyr Thr Ile Tyr Val Ile Ala Leu Lys Asn Asn Gln Lys Ser Glu     1970                1975                1980 Pro Leu Ile Gly Arg Lys Lys Thr Asp Glu Leu Pro Gln Leu Val     1985                1990                1995 Thr Leu Pro His Pro Asn Leu His Gly Pro Glu Ile Leu Asp Val     2000                2005                2010 Pro Ser Thr Val Gln Lys Thr Pro Phe Val Thr His Pro Gly Tyr     2015                2020                2025 Asp Thr Gly Asn Gly Ile Gln Leu Pro Gly Thr Ser Gly Gln Gln     2030                2035                2040 Pro Ser Val Gly Gln Gln Met Ile Phe Glu Glu His Gly Phe Arg     2045                2050                2055 Arg Thr Thr Pro Pro Thr Thr Ala Thr Pro Ile Arg His Arg Pro     2060                2065                2070 Arg Pro Tyr Pro Pro Asn Val Gly Glu Glu Ile Gln Ile Gly His     2075                2080                2085 Ile Pro Arg Glu Asp Val Asp Tyr His Leu Tyr Pro His Gly Pro     2090                2095                2100 Gly Leu Asn Pro Asn Ala Ser Thr Gly Gln Glu Ala Leu Ser Gln     2105                2110                2115 Thr Thr Ile Ser Trp Ala Pro Phe Gln Asp Thr Ser Glu Tyr Ile     2120                2125                2130 Ile Ser Cys His Pro Val Gly Thr Asp Glu Glu Pro Leu Gln Phe     2135                2140                2145 Arg Val Pro Gly Thr Ser Thr Ser Ala Thr Leu Thr Gly Leu Thr     2150                2155                2160 Arg Gly Ala Thr Tyr Asn Val Ile Val Glu Ala Leu Lys Asp Gln     2165                2170                2175 Gln Arg His Lys Val Arg Glu Glu Val Val Thr Val Gly Asn Ser     2180                2185                2190 Val Asn Glu Gly Leu Asn Gln Pro Thr Asp Asp Ser Cys Phe Asp     2195                2200                2205 Pro Tyr Thr Val Ser His Tyr Ala Val Gly Asp Glu Trp Glu Arg     2210                2215                2220 Met Ser Glu Ser Gly Phe Lys Leu Leu Cys Gln Cys Leu Gly Phe     2225                2230                2235 Gly Ser Gly His Phe Arg Cys Asp Ser Ser Arg Trp Cys His Asp     2240                2245                2250 Asn Gly Val Asn Tyr Lys Ile Gly Glu Lys Trp Asp Arg Gln Gly     2255                2260                2265 Glu Asn Gly Gln Met Met Ser Cys Thr Cys Leu Gly Asn Gly Lys     2270                2275                2280 Gly Glu Phe Lys Cys Asp Pro His Glu Ala Thr Cys Tyr Asp Asp     2285                2290                2295 Gly Lys Thr Tyr His Val Gly Glu Gln Trp Gln Lys Glu Tyr Leu     2300                2305                2310 Gly Ala Ile Cys Ser Cys Thr Cys Phe Gly Gly Gln Arg Gly Trp     2315                2320                2325 Arg Cys Asp Asn Cys Arg Arg Pro Gly Gly Glu Pro Ser Pro Glu     2330                2335                2340 Gly Thr Thr Gly Gln Ser Tyr Asn Gln Tyr Ser Gln Arg Tyr His     2345                2350                2355 Gln Arg Thr Asn Thr Asn Val Asn Cys Pro Ile Glu Cys Phe Met     2360                2365                2370 Pro Leu Asp Val Gln Ala Asp Arg Glu Asp Ser Arg Glu     2375                2380                2385

The corresponding nucleotide sequence encoding the full-length human fibronectin protein is provided as SEQ ID NO:2 below (NCBI Reference Sequence No. NM_212482.1, which is hereby incorporated by reference in its entirety).

SEQ ID NO: 2 Human Fibronectin gcccgcgccg gctgtgctgc acagggggag gagagggaac cccaggcgcg agcgggaaga   60 ggggacctgc agccacaact tctctggtcc tctgcatccc ttctgtccct ccacccgtcc  120 ccttccccac cctctggccc ccaccttctt ggaggcgaca acccccggga ggcattagaa  180 gggatttttc ccgcaggttg cgaagggaag caaacttggt ggcaacttgc ctcccggtgc  240 gggcgtctct cccccaccgt ctcaacatgc ttaggggtcc ggggcccggg ctgctgctgc  300 tggccgtcca gtgcctgggg acagcggtgc cctccacggg agcctcgaag agcaagaggc  360 aggctcagca aatggttcag ccccagtccc cggtggctgt cagtcaaagc aagcccggtt  420 gttatgacaa tggaaaacac tatcagataa atcaacagtg ggagcggacc tacctaggca  480 atgcgttggt ttgtacttgt tatggaggaa gccgaggttt taactgcgag agtaaacctg  540 aagctgaaga gacttgcttt gacaagtaca ctgggaacac ttaccgagtg ggtgacactt  600 atgagcgtcc taaagactcc atgatctggg actgtacctg catcggggct gggcgaggga  660 gaataagctg taccatcgca aaccgctgcc atgaaggggg tcagtcctac aagattggtg  720 acacctggag gagaccacat gagactggtg gttacatgtt agagtgtgtg tgtcttggta  780 atggaaaagg agaatggacc tgcaagccca tagctgagaa gtgttttgat catgctgctg  840 ggacttccta tgtggtcgga gaaacgtggg agaagcccta ccaaggctgg atgatggtag  900 attgtacttg cctgggagaa ggcagcggac gcatcacttg cacttctaga aatagatgca  960 acgatcagga cacaaggaca tcctatagaa ttggagacac ctggagcaag aaggataatc 1020 gaggaaacct gctccagtgc atctgcacag gcaacggccg aggagagtgg aagtgtgaga 1080 ggcacacctc tgtgcagacc acatcgagcg gatctggccc cttcaccgat gttcgtgcag 1140 ctgtttacca accgcagcct cacccccagc ctcctcccta tggccactgt gtcacagaca 1200 gtggtgtggt ctactctgtg gggatgcagt ggctgaagac acaaggaaat aagcaaatgc 1260 tttgcacgtg cctgggcaac ggagtcagct gccaagagac agctgtaacc cagacttacg 1320 gtggcaactc aaatggagag ccatgtgtct taccattcac ctacaatggc aggacgttct 1380 actcctgcac cacagaaggg cgacaggacg gacatctttg gtgcagcaca acttcgaatt 1440 atgagcagga ccagaaatac tctttctgca cagaccacac tgttttggtt cagactcgag 1500 gaggaaattc caatggtgcc ttgtgccact tccccttcct atacaacaac cacaattaca 1560 ctgattgcac ttctgagggc agaagagaca acatgaagtg gtgtgggacc acacagaact 1620 atgatgccga ccagaagttt gggttctgcc ccatggctgc ccacgaggaa atctgcacaa 1680 ccaatgaagg ggtcatgtac cgcattggag atcagtggga taagcagcat gacatgggtc 1740 acatgatgag gtgcacgtgt gttgggaatg gtcgtgggga atggacatgc attgcctact 1800 cgcagcttcg agatcagtgc attgttgatg acatcactta caatgtgaac gacacattcc 1860 acaagcgtca tgaagagggg cacatgctga actgtacatg cttcggtcag ggtcggggca 1920 ggtggaagtg tgatcccgtc gaccaatgcc aggattcaga gactgggacg ttttatcaaa 1980 ttggagattc atgggagaag tatgtgcatg gtgtcagata ccagtgctac tgctatggcc 2040 gtggcattgg ggagtggcat tgccaacctt tacagaccta tccaagctca agtggtcctg 2100 tcgaagtatt tatcactgag actccgagtc agcccaactc ccaccccatc cagtggaatg 2160 caccacagcc atctcacatt tccaagtaca ttctcaggtg gagacctaaa aattctgtag 2220 gccgttggaa ggaagctacc ataccaggcc acttaaactc ctacaccatc aaaggcctga 2280 agcctggtgt ggtatacgag ggccagctca tcagcatcca gcagtacggc caccaagaag 2340 tgactcgctt tgacttcacc accaccagca ccagcacacc tgtgaccagc aacaccgtga 2400 caggagagac gactcccttt tctcctcttg tggccacttc tgaatctgtg accgaaatca 2460 cagccagtag ctttgtggtc tcctgggtct cagcttccga caccgtgtcg ggattccggg 2520 tggaatatga gctgagtgag gagggagatg agccacagta cctggatctt ccaagcacag 2580 ccacttctgt gaacatccct gacctgcttc ctggccgaaa atacattgta aatgtctatc 2640 agatatctga ggatggggag cagagtttga tcctgtctac ttcacaaaca acagcgcctg 2700 atgcccctcc tgacccgact gtggaccaag ttgatgacac ctcaattgtt gttcgctgga 2760 gcagacccca ggctcccatc acagggtaca gaatagtcta ttcgccatca gtagaaggta 2820 gcagcacaga actcaacctt cctgaaactg caaactccgt caccctcagt gacttgcaac 2880 ctggtgttca gtataacatc actatctatg ctgtggaaga aaatcaagaa agtacacctg 2940 ttgtcattca acaagaaacc actggcaccc cacgctcaga tacagtgccc tctcccaggg 3000 acctgcagtt tgtggaagtg acagacgtga aggtcaccat catgtggaca ccgcctgaga 3060 gtgcagtgac cggctaccgt gtggatgtga tccccgtcaa cctgcctggc gagcacgggc 3120 agaggctgcc catcagcagg aacacctttg cagaagtcac cgggctgtcc cctggggtca 3180 cctattactt caaagtcttt gcagtgagcc atgggaggga gagcaagcct ctgactgctc 3240 aacagacaac caaactggat gctcccacta acctccagtt tgtcaatgaa actgattcta 3300 ctgtcctggt gagatggact ccacctcggg cccagataac aggataccga ctgaccgtgg 3360 gccttacccg aagaggacag cccaggcagt acaatgtggg tccctctgtc tccaagtacc 3420 cactgaggaa tctgcagcct gcatctgagt acaccgtatc cctcgtggcc ataaagggca 3480 accaagagag ccccaaagcc actggagtct ttaccacact gcagcctggg agctctattc 3540 caccttacaa caccgaggtg actgagacca ccattgtgat cacatggacg cctgctccaa 3600 gaattggttt taagctgggt gtacgaccaa gccagggagg agaggcacca cgagaagtga 3660 cttcagactc aggaagcatc gttgtgtccg gcttgactcc aggagtagaa tacgtctaca 3720 ccatccaagt cctgagagat ggacaggaaa gagatgcgcc aattgtaaac aaagtggtga 3780 caccattgtc tccaccaaca aacttgcatc tggaggcaaa ccctgacact ggagtgctca 3840 cagtctcctg ggagaggagc accaccccag acattactgg ttatagaatt accacaaccc 3900 ctacaaacgg ccagcaggga aattctttgg aagaagtggt ccatgctgat cagagctcct 3960 gcacttttga taacctgagt cccggcctgg agtacaatgt cagtgtttac actgtcaagg 4020 atgacaagga aagtgtccct atctctgata ccatcatccc agaggtgccc caactcactg 4080 acctaagctt tgttgatata accgattcaa gcatcggcct gaggtggacc ccgctaaact 4140 cttccaccat tattgggtac cgcatcacag tagttgcggc aggagaaggt atccctattt 4200 ttgaagattt tgtggactcc tcagtaggat actacacagt cacagggctg gagccgggca 4260 ttgactatga tatcagcgtt atcactctca ttaatggcgg cgagagtgcc cctactacac 4320 tgacacaaca aacggctgtt cctcctccca ctgacctgcg attcaccaac attggtccag 4380 acaccatgcg tgtcacctgg gctccacccc catccattga tttaaccaac ttcctggtgc 4440 gttactcacc tgtgaaaaat gaggaagatg ttgcagagtt gtcaatttct ccttcagaca 4500 atgcagtggt cttaacaaat ctcctgcctg gtacagaata tgtagtgagt gtctccagtg 4560 tctacgaaca acatgagagc acacctctta gaggaagaca gaaaacaggt cttgattccc 4620 caactggcat tgacttttct gatattactg ccaactcttt tactgtgcac tggattgctc 4680 ctcgagccac catcactggc tacaggatcc gccatcatcc cgagcacttc agtgggagac 4740 ctcgagaaga tcgggtgccc cactctcgga attccatcac cctcaccaac ctcactccag 4800 gcacagagta tgtggtcagc atcgttgctc ttaatggcag agaggaaagt cccttattga 4860 ttggccaaca atcaacagtt tctgatgttc cgagggacct ggaagttgtt gctgcgaccc 4920 ccaccagcct actgatcagc tgggatgctc ctgctgtcac agtgagatat tacaggatca 4980 cttacggaga gacaggagga aatagccctg tccaggagtt cactgtgcct gggagcaagt 5040 ctacagctac catcagcggc cttaaacctg gagttgatta taccatcact gtgtatgctg 5100 tcactggccg tggagacagc cccgcaagca gcaagccaat ttccattaat taccgaacag 5160 aaattgacaa accatcccag atgcaagtga ccgatgttca ggacaacagc attagtgtca 5220 agtggctgcc ttcaagttcc cctgttactg gttacagagt aaccaccact cccaaaaatg 5280 gaccaggacc aacaaaaact aaaactgcag gtccagatca aacagaaatg actattgaag 5340 gcttgcagcc cacagtggag tatgtggtta gtgtctatgc tcagaatcca agcggagaga 5400 gtcagcctct ggttcagact gcagtaacca acattgatcg ccctaaagga ctggcattca 5460 ctgatgtgga tgtcgattcc atcaaaattg cttgggaaag cccacagggg caagtttcca 5520 ggtacagggt gacctactcg agccctgagg atggaatcca tgagctattc cctgcacctg 5580 atggtgaaga agacactgca gagctgcaag gcctcagacc gggttctgag tacacagtca 5640 gtgtggttgc cttgcacgat gatatggaga gccagcccct gattggaacc cagtccacag 5700 ctattcctgc accaactgac ctgaagttca ctcaggtcac acccacaagc ctgagcgccc 5760 agtggacacc acccaatgtt cagctcactg gatatcgagt gcgggtgacc cccaaggaga 5820 agaccggacc aatgaaagaa atcaaccttg ctcctgacag ctcatccgtg gttgtatcag 5880 gacttatggt ggccaccaaa tatgaagtga gtgtctatgc tcttaaggac actttgacaa 5940 gcagaccagc tcagggagtt gtcaccactc tggagaatgt cagcccacca agaagggctc 6000 gtgtgacaga tgctactgag accaccatca ccattagctg gagaaccaag actgagacga 6060 tcactggctt ccaagttgat gccgttccag ccaatggcca gactccaatc cagagaacca 6120 tcaagccaga tgtcagaagc tacaccatca caggtttaca accaggcacc gactacaaga 6180 tctacctgta caccttgaat gacaatgctc ggagctcccc tgtggtcatc gacgcctcca 6240 ctgccattga tgcaccatcc aacctgcgtt tcctggccac cacacccaat tccttgctgg 6300 tatcatggca gccgccacgt gccaggatta ccggctacat catcaagtat gagaagcctg 6360 ggtctcctcc cagagaagtg gtccctcggc cccgccctgg tgtcacagag gctactatta 6420 ctggcctgga accgggaacc gaatatacaa tttatgtcat tgccctgaag aataatcaga 6480 agagcgagcc cctgattgga aggaaaaaga cagacgagct tccccaactg gtaacccttc 6540 cacaccccaa tcttcatgga ccagagatct tggatgttcc ttccacagtt caaaagaccc 6600 ctttcgtcac ccaccctggg tatgacactg gaaatggtat tcagcttcct ggcacttctg 6660 gtcagcaacc cagtgttggg caacaaatga tctttgagga acatggtttc aggcggacca 6720 caccgcccac aacggccacc cccataaggc ataggccaag accatacccg ccgaatgtag 6780 gtgaggaaat ccaaattggt cacatcccca gggaagatgt agactatcac ctgtacccac 6840 acggtccggg actcaatcca aatgcctcta caggacaaga agctctctcC cagacaacca 6900 tctcatgggc cccattccag gacacttctg agtacatcat ttcatgtcat cctgttggca 6960 ctgatgaaga acccttacag ttcagggttc ctggaacttc taccagtgcc actctgacag 7020 gcctcaccag aggtgccacc tacaacatca tagtggaggc actgaaagac cagcagaggc 7080 ataaggttcg ggaagaggtt gttaccgtgg gcaactctgt caacgaaggc ttgaaccaac 7140 ctacggatga ctcgtgcttt gacccctaca cagtttccca ttatgccgtt ggagatgagt 7200 gggaacgaat gtctgaatca ggctttaaac tgttgtgcca gtgcttaggc tttggaagtg 7260 gtcatttcag atgtgattca tctagatggt gccatgacaa tggtgtgaac tacaagactg 7320 gagagaagtg ggaccgtcag ggagaaaatg gccagatgat gagctgcaca tgtcttggga 7380 acggaaaagg agaattcaag tgtgaccctc atgaggcaac gtgttatgat gatgggaaga 7440 cataccacgt aggagaacag tggcagaagg aatatctcgg tgccatttgc tcctgcacat 7500 gctttggagg ccagcggggc tggcgctgtg acaactgccg cagacctggg ggtgaaccca 7560 gtcccgaagg cactactggc cagtcctaca accagtattc tcagagatac catcagagaa 7620 caaacactaa tgttaattgc ccaattgagt gcttcatgcc tttagatgta caggctgaca 7680 gagaagattc ccgagagtaa atcatctttc caatccagag gaacaagcat gtctctctgc 7740 caagatccat ctaaactgga gtgatgttag cagacccagc ttagagttct tctttctttc 7800 ttaagccctt tgctctggag gaagttctcc agcttcagct caactcacag cttctccaag 7860 catcaccctg ggagtttcct gagggttttc tcataaatga gggctgcaca ttgcctgttc 7920 tgcttcgaag tattcaatac cgctcagtat tttaaatgaa gtgattctaa gatttggttt 7980 gggatcaata ggaaagcata tgcagccaac caagatgcaa atgttttgaa atgatatgac 8040 caaaatttta agtaggaaag tcacccaaac acttctgctt tcacttaagt gtctggcccg 8100 caatactgta ggaacaagca tgatcttgtt actgtgatat tttaaatatc cacagtactc 8160 actttttcca aatgatccta gtaattgcct agaaatatct ttctcttacc tgttatttat 8220 caatttttcc cagtattttt atacggaaaa aattgtattg aaaacactta gtatgcagtt 8280 gataagagga atttggtata attatggtgg gtgattattt tttatactgt atgtgccaaa 8340 gctttactac tgtggaaaga caactgtttt aataaaagat ttacattcca caacttgaag 8400 ttcatctatt tgatataaga caccttcggg ggaaataatt cctgtgaata ttctttttca 8460 attcagcaaa catttgaaaa tctatgatgt gcaagtctaa ttgttgattt cagtacaaga 8520 ttttctaaat cagttgctac aaaaactgat tggtttttgt cacttcatct cttcactaat 8580 ggagatagct ttacactttc tgctttaata gatttaagtg gaccccaata tttattaaaa 8640 ttgctagttt accgttcaga agtataatag aaataatctt tagttgctct tttctaacca 8700 ttgtaattct tcccttcttc cctccacctt tccttcattg aataaacctc tgttcaaaga 8760 gattgcctgc aagggaaata aaaatgacta agatattaaa aaaaaaaaaa aaaaa 8815

In accordance with this aspect of the invention, the recombinant fibronectin peptide mimetic comprises at least a portion of the type III heparin binding domain FNIII1H. FNIII1H is the C-terminal fragment of FNIII1 that extends from amino acid residues 628-704 of SEQ ID NO:1.

The at least a portion of the FNIII1H domain comprises, at a minimum, a heparin binding sequence having an amino acid sequence of Xaa-Trp-Xaa-Pro-Xaa (SEQ ID NO: 12), where Xaa is any charged amino acid. In one embodiment of the present invention, this portion of the recombinant fibronectin peptide mimetic contains more than one heparin binding sequences. In accordance with this embodiment, multiple heparin binding sequences may be the same (i.e., repeating sequence), or comprise different heparin binding sequences.

In one embodiment of the present invention, the heparin binding sequence has an amino acid sequence of Arg-Trp-Arg-Pro-Lys (SEQ ID NO:13), corresponding to amino acids 644-648 of the full-length human fibronectin amino acid sequence (SEQ ID NO: 1) (or amino acid residues 613-617 of the mature fibronectin protein lacking the 31-amino acid leader sequence). Other embodiments include a heparin binding sequence of SEQ ID NO:12 having one or more additional amino acid residues at either its N-terminal side or its C-terminal side, or both.

In another embodiment of the present invention, the at least a portion of the FNIII1H comprises an amino acid sequence corresponding to amino acids 628-704 of SEQ ID NO: 1.

The at least a portion of the type III integrin binding domain of the recombinant fibronectin peptide mimetic of the present invention comprises, at a minimum, an integrin binding sequence. In one embodiment of the present invention, this portion of the recombinant fibronectin peptide mimetic comprises more than one integrin binding sequence. In accordance with this embodiment, the multiple integrin binding sequences may be the same (i.e., repeating sequences) or different sequences. This portion can be linked directly to the type III heparin binding domain portion. Alternatively, one or more linker amino acid residues can be incorporated at the junction of these portions. Suitable linker amino acids include, with out limitation, one or more serine or glycine residues.

The at least a portion of the type III integrin binding domain can be derived from the FNIII8 (amino acid residues 1266-1356 of SEQ ID NO:1), FNIII9 (amino acid residues 1357-1446 of SEQ ID NO:1), or FNIII10 (amino acids 1447-1536 of SEQ ID NO: 1) modules alone or in any combination. In one embodiment of the present invention, this portion does not include the FNIII9 module in its entirety when the FNIII8 and FNIII10 modules are incorporated in their entirety. In accordance with this embodiment of the present invention, this portion may comprise less than 85 amino acid residues of the FNIII9 module, less than 75 amino acid residues of the FNIII9 module, less than 65 amino acid residues of the FNIII9 module, less than 55 amino acid residues of the FNIII9 module, less than 45 amino acid residues of the FNIII9 module, less than 35 amino acid residues of the FNIII9 module, less than 25 amino acid residues of the FNIII9 module, less than 15 amino acid residues of the FNIII9 module, less than 5 amino acid residues of the FNIII9 module, or no amino acid residue of the FNIII9 module.

In one embodiment of the present invention, the portion of the type III integrin binding domain comprises the FNIII8 module, or a portion thereof, linked to the FNIII10 module, or a portion thereof. Consistent with this embodiment of the present invention, the portion of the type III integrin binding domain has an amino acid sequence corresponding to amino acids 1266-1356 of SEQ ID NO:1 (FNIII8) linked to amino acids 1447-1536 of SEQ ID NO: 1 (FNIII10). As described infra, the amino acid residues of the FNIII8 module can be linked directly to the FNIII10 module (i.e., via an inframe gene fusion). Alternatively, linker amino acid residues can be incorporated into the junction. Suitable linker amino acid residues include one or more serine and/or glycine amino acid residues.

The three-dimensional structure of FnIII has been determined by NMR (Main et al., “The Three-Dimensional Structure of the Tenth Type III Module of FIbronectin: An Insight into RGD-Mediated Interactions,” Cell 71:671-678 (1992), which is hereby incorporated by reference in its entirety) and by X-ray crystallography (Leahy et al, “Structure of a Fibronectin Type III Domain From Tenascin Phased by MAD Analysis of the Selenomethionlyl Protein,” Science 258:987-991 (1992); Dickinson et al, “Crystal Structure of the Tenth Type III Cell Adhesion Module of Human Fibronectin,” J. Mol. Biol. 236: 1079-1092 (1994), which are hereby incorporated by reference in their entirety).

Both the eighth and tenth type III modules of fibronectin have a fold similar to that of immunoglobulin domains, with seven β strands forming two antiparallel β sheets, which pack against each other (Main et al, “The Three-Dimensional Structure of the Tenth Type III Module of Fibronectin: An Insight into RGD-Mediated Interactions,” Cell 71:671-678 (1992); Craig et al., “Comparison of the Early Stages of Forced Unfolding for Fibronectin Type III Modules,” Proc. Nat'l Acad. Sci. U.S.A. 98(10):5590-5595 (2001), each of which is hereby incorporated by reference in its entirety). One β sheet contains the residues of the A, B, and E strands, and the other β sheet contains the residues of the C, D, F, and G strands. The majority of the conserved residues contribute to the hydrophobic core, with the invariant hydrophobic residues Trp-22 and Tyr-68 lying toward the N-terminal and C-terminal ends of the core, respectively. The β strands are much less flexible and appear to provide a rigid framework upon which functional, flexible loops can be built. The topology is similar to that of immunoglobulin C domains. As a result, this molecule has been proven to be a powerful and versatile molecular scaffold for the generation of binding proteins, termed “monobodies,” with affinities in the nanomolar range (Koide et al, “Monobodies: Antibody Mimics Based on the Scaffold of the Fibronectin Type III Domain,” Methods Mol Biol. 352:95-109 (2007); Richards et al, “Engineered Fibronectin Type III Domain with a RGDWXE Sequence Binds with Enhanced Affinity and Specificity to Human α_(v)β₃ Integrin,” J Mol Biol. 326(5): 1475-88 (2003), which are hereby incorporated by reference in their entirety). The β-strand domain sequences A, B, C, D, E, F, and G of the type III modules of fibronectin is conserved among mammals generally.

The FNIII scaffolds are very stable and easy to produce in large quantities suitable for recombinant expression and purification. Thus, the fibronectin peptide mimetic of the present invention can include FNIII8 or FNIII10-derived polypeptides that include at least two β-strand domain sequences with a loop region sequence linked between adjacent β-strand domain sequences and optionally, an N-terminal tail of at least about 2 amino acids, a C-terminal tail of at least about 2 amino acids, or both. The fibronectin peptide mimetic of the present invention can include the β-strand domain sequences A, B, C, D, E, F, and G of a wild-type mammalian fibronectin Fn3 domain with loop region sequences AB, BC, CD, DE, EF, and FG linked between adjacent β-strand domain sequences. The fibronectin peptide mimetic also optionally includes an N-terminal tail of at least about 2 amino acids, a C-terminal tail of at least about 2 amino acids, or both.

In certain embodiments, at least one loop region sequence, the N-terminal tail, or the C-terminal tail, or combinations thereof, comprises a modified amino acid sequence which varies by deletion, insertion, or replacement of at least two amino acids from a corresponding loop region in the wild-type mammalian FNIII domain of fibronectin, and affords a functional amino acid sequence that enhances the wound healing capability of the larger peptide molecule.

One example of this is the modification of a loop region of the FNIII8 domain to include an integrin-binding sequence (e.g., RGD) derived from the FNIII10 domain as described in the accompanying examples.

In certain embodiments, it may be desirable to insert multiple heparin-binding domains or integrin-binding sequences into multiple (i.e., different) loops of the FNIII domains present in the fibronectin peptide mimetic of the present invention.

An exemplary fibronectin peptide mimetic of the present invention comprising the FNIII8 and FNIII10 modules is FNIII1H,8,10, having an amino acid sequence of SEQ ID NO: 3 as shown below (also shown schematically as peptide mimetic #2 in FIG. 1A). This sequence corresponds to amino acid residues 628-704, 1266-1356, and 1447-1536 of the full-length human fibronectin (SEQ ID NO:1).

SEQ ID NO: 3 FNIII1H, 8, 10 Ile Gln Trp Asn Ala Pro Gln Pro Ser His Ile Ser Lys Tyr Ile Leu 1               5                   10                  15 Arg Trp Arg Pro Lys Asn Ser Val Gly Arg Trp Lys Glu Ala Thr Ile             20                  25                  30 Pro Gly His Leu Asn Ser Tyr Thr Ile Lys Gly Leu Lys Pro Gly Val         35                  40                  45 Val Tyr Glu Gly Gln Leu Ile Ser Ile Gln Gln Tyr Gly His Gln Glu     50                  55                  60 Val Thr Arg Phe Asp Phe Thr Thr Thr Ser Thr Ser Thr Ala Val Pro 65                  70                  75                  80 Pro Pro Thr Asp Leu Arg Phe Thr Asn Ile Gly Pro Asp Thr Met Arg                 85                  90                  95 Val Thr Trp Ala Pro Pro Pro Ser Ile Asp Leu Thr Asn Phe Leu Val             100                 105                 110 Arg Tyr Ser Pro Val Lys Asn Glu Glu Asp Val Ala Glu Leu Ser Ile         115                 120                 125 Ser Pro Ser Asp Asn Ala Val Val Leu Thr Asn Leu Leu Pro Gly Thr     130                 135                 140 Glu Tyr Val Val Ser Val Ser Ser Val Tyr Glu Gln His Glu Ser Thr 145                 150                 155                 160 Pro Leu Arg Gly Arg Gln Lys Thr Val Ser Asp Val Pro Arg Asp Leu                 165                 170                 175 Glu Val Val Ala Ala Thr Pro Thr Ser Leu Leu Ile Ser Trp Asp Ala             180                 185                 190 Pro Ala Val Thr Val Arg Tyr Tyr Arg Ile Thr Tyr Gly Glu Thr Gly         195                 200                 205 Gly Asn Ser Pro Val Gln Glu Phe Thr Val Pro Gly Ser Lys Ser Thr     210                 215                 220 Ala Thr Ile Ser Gly Leu Lys Pro Gly Val Asp Tyr Thr Ile Thr Val 225                 230                 235                 240 Tyr Ala Val Thr Gly Arg Gly Asp Ser Pro Ala Ser Ser Lys Pro Ile                 245                 250                 255 Ser Ile

Nucleic acid molecules encoding FNIII1H,8,10 comprise a nucleotide sequence of SEQ ID NO: 4 or SEQ ID NO: 5 as shown below. The nucleotide sequence of SEQ ID NO:4 encodes glycine and serine amino acid residues linking the FNII1H and FNIII8 modules, i.e., it encodes a sequence that differs from SEQ ID NO: 3 by the addition of two glycine/serine residues between the threonine and alanine residues at positions 77 and 78. The linker codons are shown in bold in SEQ ID NO:4. No amino acid linkers were incorporated at the FNIII8 and FNIII10 junction. The nucleotide sequence of SEQ ID NO:5 does not encode any linking amino acid residues.

SEQ ID NO: 4 FNIII1H, 8, 10 atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatcagcat ccagcagtac 180 ggccaccaag aagtgactcg ctttgacttc accaccacca gcaccagcac aggatctgct 240 gttcctcctc ccactgacct gcgattcacc aacattggtc cagacaccat gcgtgtcacc 300 tgggctccac ccccatccat tgatttaacc aacttcctgg tgcgttactc acctgtgaaa 360 aatgaggaag atgttgcaga gttgtcaatt tctccttcag acaatgcagt ggtcttaaca 420 aatctcctgc ctggtacaga atatgtagtg agtgtctcca gtgtctacga acaacatgag 480 agcacacctc ttagaggaag acagaaaaca gtttctgatg ttccgaggga cctggaagtt 540 gttgctgcga cccccaccag cctactgatc agctgggatg ctcctgctgt cacagtgaga 600 tattacagga tcacttacgg agaaacagga ggaaatagcc ctgtccagga gttcactgtg 660 cctgggagca agtctacagc taccatcagc ggccttaaac ctggagttga ttataccatc 720 actgtgtatg ctgtcactgg ccgtggagac agccccgcaa gcagcaagcc aatttccatt 780 aattaccgaa ca 792 SEQ ID NO: 5 FNIII1H, 8, 10 atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatcagcat ccagcagtac 180 ggccaccaag aagtgactcg ctttgacttc accaccacca gcaccagcac agctgttcct 240 cctcccactg acctgcgatt caccaacatt ggtccagaca ccatgcgtgt cacctgggct 300 ccacccccat ccattgattt aaccaacttc ctggtgcgtt actcacctgt gaaaaatgag 360 gaagatgttg cagagttgtc aatttctcct tcagacaatg cagtggtctt aacaaatctc 420 ctgcctggta cagaatatgt agtgagtgtc tccagtgtct acgaacaaca tgagagcaca 480 cctcttagag gaagacagaa aacagtttct gatgttccga gggacctgga agttgttgct 540 gcgaccccca ccagcctact gatcagctgg gatgctcctg ctgtcacagt gagatattac 600 aggatcactt acggagaaac aggaggaaat agccctgtcc aggagttcac tgtgcctggg 660 agcaagtcta cagctaccat cagcggcctt aaacctggag ttgattatac catcactgtg 720 tatgctgtca ctggccgtgg agacagcccc gcaagcagca agccaatttc cattaattac 780 cgaaca 786

In another embodiment of the present invention, the at least a portion of the type III integrin binding domain comprises the minimal RGD integrin binding sequence. An exemplary RGD integrin binding sequence is the RGD sequence of RGDSPAS (SEQ ID NO: 14) present in the FNIII10 module. Alternatively, the RGD integrin binding sequence can be heterologous to the type III integrin-binding domain of fibronectin (i.e., an RGD integrin binding sequence that is not present in SEQ ID NO:1). Exemplary RGD integrin binding sequences include, without limitation, GRGD (SEQ ID NO: 15); GRGDS (SEQ ID NO: 16); GRGDSPK (SEQ ID NO: 17); GRGDTP (SEQ ID NO: 18); SDGRGRGDS (SEQ ID NO: 19); RGDS (SEQ ID NO: 20); RGDSPASSKP (SEQ ID NO: 21); RRRRRRGDSPK (SEQ ID NO: 22); and G(dR)GDSPASSK (dR is D-arginine) (SEQ ID NO: 23), or functional variants thereof. An exemplary fibronectin peptide mimetic of the present invention where the type III integrin binding domain comprises an RGD sequence is FNIII1H^(RGD), having an amino acid sequence of SEQ ID NO: 6 as shown below. This amino acid sequence corresponds to amino acid residues 628-685, 1523-1530, and 690-704 of the full-length human fibronectin (SEQ ID NO:1).

SEQ ID NO: 6 FNIII1H^(RGD) Ile Gln Trp Asn Ala Pro Gln Pro Ser His Ile Ser Lys Tyr Ile Leu 1               5                   10                  15 Arg Trp Arg Pro Lys Asn Ser Val Gly Arg Trp Lys Glu Ala Thr Ile             20                  25                  30 Pro Gly His Leu Asn Ser Tyr Thr Ile Lys Gly Leu Lys Pro Gly Val         35                  40                  45 Val Tyr Glu Gly Gln Leu Ile Ser Ile Gln Gly Arg Gly Asp Ser Pro     50                  55                  60 Ala Ser Gln Glu Val Thr Arg Phe Asp Phe Thr Thr Thr Ser Thr Ser 65                  70                  75                  80 Thr

Nucleic acid molecules encoding FNIII1H,^(RGD) comprise the nucleotide sequence of SEQ ID NO:7 or SEQ ID NO: 8 shown below. The nucleotide sequence of SEQ ID NO:7 contains a three codon sequence (underlined) containing five silent base changes (bold). The first four base changes introduce a ClaI site (ATCGAT) to facilitate cloning of the downstream sequence; the final base change renders the ClaI site methylation insensitive. The nucleotide sequence of SEQ ID NO:8 does not contain these five base changes.

SEQ ID NO: 7 FNIII1H,^(RGD) atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatatcgat t cagggccgt 180 ggagactcgc cggcaagcca agaagtgact cgctttgact tcaccaccac cagcaccagc 240 aca 243 SEQ ID NO: 8 FNIII1H,^(RGD) atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatcagcat ccagggccgt 180 ggagactcgc cggcaagcca agaagtgact cgctttgact tcaccaccac cagcaccagc 240 aca 243

In yet another embodiment of the present invention, the at least a portion of the type III integrin binding domain comprises the FNIII8 module containing an RGD sequence. The RGD sequence can be derived from the FNIII10 module or it can be heterologous to the type III integrin binding domain. An exemplary fibronectin peptide mimetic comprising an FNIII8 module containing an RGD sequence is FNIII1H,8^(RGD), having an amino acid sequence of SEQ ID NO: 9 below (also shown schematically in FIG. 1 as mimetic peptide #6). This amino acid sequence corresponds to amino acids residues 628-704; 1266-1342; 1523-1530; 1347-1356 of the full-length human fibronectin (SEQ ID NO:1).

SEQ ID NO: 9 FNIII1H, 8^(RGD) Ile Gln Trp Asn Ala Pro Gln Pro Ser His Ile Ser Lys Tyr Ile Leu 1               5                   10                  15 Arg Trp Arg Pro Lys Asn Ser Val Gly Arg Trp Lys Glu Ala Thr Ile             20                  25                  30 Pro Gly His Leu Asn Ser Tyr Thr Ile Lys Gly Leu Lys Pro Gly Val         35                  40                  45 Val Tyr Glu Gly Gln Leu Ile Ser Ile Gln Gln Tyr Gly His Gln Glu     50                  55                  60 Val Thr Arg Phe Asp Phe Thr Thr Thr Ser Thr Ser Thr Ala Val Pro 65                  70                  75                  80 Pro Pro Thr Asp Leu Arg Phe Thr Asn Ile Gly Pro Asp Thr Met Arg                 85                  90                  95 Val Thr Trp Ala Pro Pro Pro Ser Ile Asp Leu Thr Asn Phe Leu Val             100                 105                 110 Arg Tyr Ser Pro Val Lys Asn Glu Glu Asp Val Ala Glu Leu Ser Ile         115                 120                 125 Ser Pro Ser Asp Asn Ala Val Val Leu Thr Asn Leu Leu Pro Gly Thr     130                 135                 140 Glu Tyr Val Val Ser Val Ser Ser Val Tyr Gly Arg Gly Asp Ser Pro 145                 150                 155                 160 Ala Ser Ser Thr Pro Leu Arg Gly Arg Gln Lys Thr                 165                 170

Nucleic acid molecules encoding FNIII1H,8^(RGD) comprise the nucleotide sequence of SEQ ID NO:10 or SEQ ID NO:11 shown below. The nucleotide sequence of SEQ ID NO:10 contains the three codon sequence (underlined) containing five silent base changes (bold) described above to introduce a ClaI site, and encodes two glycine and serine residues (underlined) linking the FNIII1H and FNIII8 modules (i.e., the glycine and serine residues are inserted between the threonine and alanine residues at positions 77 and 78 of SEQ ID NO:9). The nucleotide sequence of SEQ ID NO:11 does not encode the ClaI site or linking amino acid residues.

SEQ ID NO: 10 FNIII1H, 8^(RGD) atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatatcgat t cagcagtac 180 ggccaccaag aagtgactcg ctttgacttc accaccacca gcaccagcac aggatctgct 240 gttcctcctc ccactgacct gcgattcacc aacattggtc cagacaccat gcgtgtcacc 300 tgggctccac ccccatccat tgatttaacc aacttcctgg tgcgttactc acctgtgaaa 360 aatgaggaag atgttgcaga gttgtcaatt tctccttcag acaatgcagt ggtcttaaca 420 aatctcctgc ctggtacaga atatgtagtg agtgtctcca gtgtctacgg ccgtggagac 480 tcgccggcaa gcagcacacc tcttagagga agacagaaaa ca 522 SEQ ID NO: 11 FNIII1H, 8^(RGD) atccagtgga atgcaccaca gccatctcac atttccaagt acattctcag gtggagacct  60 aaaaattctg taggccgttg gaaggaagct accataccag gccacttaaa ctcctacacc 120 atcaaaggcc tgaagcctgg tgtggtatac gagggccagc tcatcagcat ccagcagtac 180 ggccaccaag aagtgactcg ctttgacttc accaccacca gcaccagcac agctgttcct 240 cctcccactg acctgcgatt caccaacatt ggtccagaca ccatgcgtgt cacctgggct 300 ccacccccat ccattgattt aaccaacttc ctggtgcgtt actcacctgt gaaaaatgag 360 gaagatgttg cagagttgtc aatttctcct tcagacaatg cagtggtctt aacaaatctc 420 ctgcctggta cagaatatgt agtgagtgtc tccagtgtct acggccgtgg agactcgccg 480 gcaagcagca cacctcttag aggaagacag aaaaca 516

The recombinant fibronectin peptide mimetic of the present invention may further comprise a targeting moiety. A targeting moiety according to the present invention functions to target the peptide mimetic to a particular cell or tissue type (e.g., signaling peptide sequence). The signaling peptide can include at least a portion of a ligand binding protein. Suitable ligand binding proteins include high-affinity antibody fragments (e.g., Fab, Fab′ and F(ab′)₂), single-chain Fv antibody fragments), nanobodies or nanobody fragments, fluorobodies, or aptamers. Other ligand binding proteins include biotin-binding proteins, lipid-binding proteins, periplasmic binding proteins, lectins, serum albumins, enzymes, phosphate and sulfate binding proteins, immunophilins, metallothionein, or various other receptor proteins. For cell specific targeting, the signaling peptide is preferably a ligand binding domain of a cell specific membrane receptor.

The recombinant fibronectin peptide mimetic of the present invention may further comprise a tag. A “tag” as used herein includes any labeling moiety that facilitates the detection/imaging, quantitation, separation, and/or purification of the recombinant peptide of the present invention. Suitable tags include purification tags, ultrasound contrast agents, radioactive or fluorescent labels, and enzymatic tags.

Purification tags, such as poly-histidine (His⁶⁻), glutathione-S-transferase (GST), or maltose-binding protein (MBP−), can assist in peptide purification or separation but can later be removed, i.e., cleaved from the peptide following recovery. Protease-specific cleavage sites can be used to facilitate the removal of the purification tag. The desired peptide mimetic product can be purified further to remove the cleaved purification tags.

Other suitable tags include ultrasound contrast agents, such as gas-filled microbubbles, that can be used for imaging and to facilitate the spatial patterning of proteins. Ultrasound contrast agents are detected using contrast-enhanced ultrasonography. Other suitable tags include radioactive labels, such as, ¹²⁵I, ¹³¹I, ¹¹¹In, or ⁹⁹TC. Methods of radiolabeling compounds, are known in the art and described in U.S. Pat. No. 5,830,431 to Srinivasan et al., which is hereby incorporated by reference in its entirety. Radioactivity is detected and quantified using a scintillation counter or autoradiography. Alternatively, the peptide can be conjugated to a fluorescent tag. Suitable fluorescent tags include, without limitation, chelates (europium chelates), fluorescein and its derivatives, rhodamine and its derivatives, dansyl, Lissamine, phycoerythrin and Texas Red. The fluorescent labels can be conjugated to the peptide using techniques disclosed in CURRENT PROTOCOLS IN IMMUNOLOGY (Coligen et al. eds., 1991), which is hereby incorporated by reference in its entirety. Fluorescence can be detected and quantified using a fluorometer.

Other suitable tags include enzyme tags. Enzymatic tags generally catalyze a chemical alteration of a chromogenic substrate which can be measured using various techniques. For example, the enzyme may catalyze a color change in a substrate, which can be measured spectrophotometrically. Alternatively, the enzyme may alter the fluorescence or chemiluminescence of the substrate. Examples of suitable enzymatic tags include luciferases (e.g., firefly luciferase and bacterial luciferase; see e.g., U.S. Pat. No. 4,737,456 to Weng et al., which is hereby incorporated by reference in its entirety), luciferin, 2,3-dihydrophthalazinediones, malate dehydrogenase, urease, peroxidases (e.g., horseradish peroxidase), alkaline phosphatase, β-galactosidase, glucoamylase, lysozyme, saccharide oxidases (e.g., glucose oxidase, galactose oxidase, and glucose-6-phosphate dehydrogenase), heterocyclic oxidases (e.g., uricase and xanthine oxidase), lactoperoxidase, microperoxidase, and the like. Techniques for conjugating enzymes to proteins and peptides are described in O'Sullivan et al., Methods for the Preparation of Enzyme—Antibody Conjugates for Use in Enzyme Immunoassay, in METHODS IN ENZYMOLOGY 147-66 (Langone et al. eds., 1981), which is hereby incorporated by reference in its entirety.

The recombinant fibronectin mimetics of the present invention may be prepared using standard methods of synthesis known in the art, including solid phase peptide synthesis (Fmoc or Boc strategies) or solution phase peptide synthesis. Alternatively, peptides of the present invention may be prepared using recombinant expression systems.

Generally, the use of recombinant expression systems involves inserting the nucleic acid molecule encoding the amino acid sequence of the desired peptide into an expression system to which the molecule is heterologous (i.e., not normally present). One or more desired nucleic acid molecules encoding a peptide mimetic of the invention may be inserted into the vector. The heterologous nucleic acid molecule is inserted into the expression system or vector in proper sense (5′→3′) orientation relative to the promoter and any other 5′ regulatory molecules, and correct reading frame.

The preparation of the nucleic acid constructs can be carried out using standard cloning procedures well known in the art as described by Joseph Sambrook et al., MOLECULAR CLONING: A LABORATORY MANUAL (Cold Springs Harbor 1989). U.S. Pat. No. 4,237,224 to Cohen and Boyer, which is hereby incorporated by reference in its entirety, describes the production of expression systems in the form of recombinant plasmids using restriction enzyme cleavage and ligation with DNA ligase. These recombinant plasmids are then introduced by means of transformation and replicated in a suitable host cell.

A variety of genetic signals and processing events that control many levels of gene expression (e.g., DNA transcription and messenger RNA (“mRNA”) translation) can be incorporated into the nucleic acid construct to maximize peptide mimetic production. For the purposes of expressing a cloned nucleic acid sequence encoding a desired peptide, it is advantageous to use strong promoters to obtain a high level of transcription. Depending upon the host system utilized, any one of a number of suitable promoters may be used. For instance, when cloning in E. coli, its bacteriophages, or plasmids, promoters such as the T7 phage promoter, lac promoter, trp promoter, recA promoter, ribosomal RNA promoter, the P_(R) and P_(L) promoters of coliphage lambda and others, including but not limited, to lacUV5, ompF, bla, lpp, and the like, may be used to direct high levels of transcription of adjacent DNA segments. Additionally, a hybrid trp-lacUV5 (tac) promoter or other E. coli promoters produced by recombinant DNA or other synthetic DNA techniques may be used to provide for transcription of the inserted nucleotide sequence. Common promoters suitable for directing expression in mammalian cells include, without limitation, SV40, MMTV, metallothionein-1, adenovirus Ela, CMV, immediate early, immunoglobulin heavy chain promoter and enhancer, and RSV-LTR.

There are other specific initiation signals required for efficient gene transcription and translation in prokaryotic cells that can be included in the nucleic acid construct to maximize peptide production. Depending on the vector system and host utilized, any number of suitable transcription and/or translation elements, including constitutive, inducible, and repressible promoters, as well as minimal 5′ promoter elements, enhancers or leader sequences may be used. For a review on maximizing gene expression see Roberts and Lauer, “Maximizing Gene Expression On a Plasmid Using Recombination In Vitro,” Methods in Enzymology 68:473-82 (1979), which is hereby incorporated by reference in its entirety.

A nucleic acid molecule encoding an isolated peptide of the present invention, a promoter molecule of choice, including, without limitation, enhancers, and leader sequences; a suitable 3′ regulatory region to allow transcription in the host, and any additional desired components, such as reporter or marker genes, are cloned into the vector of choice using standard cloning procedures in the art, such as described in Joseph Sambrook et al., MOLECULAR CLONING: A LABORATORY MANUAL (Cold Springs Harbor 1989); Frederick M. Ausubel, SHORT PROTOCOLS IN MOLECULAR BIOLOGY (Wiley 1999), and U.S. Pat. No. 4,237,224 to Cohen and Boyer, which are hereby incorporated by reference in their entirety.

Once the nucleic acid molecule encoding the peptide mimetic has been cloned into an expression vector, it is ready to be incorporated into a host. Recombinant molecules can be introduced into cells, without limitation, via transfection (if the host is a eukaryote), transduction, conjugation, mobilization, or electroporation, lipofection, protoplast fusion, mobilization, or particle bombardment, using standard cloning procedures known in the art, as described by JOSEPH SAMBROOK et al., MOLECULAR CLONING: A LABORATORY MANUAL (Cold Springs Harbor 1989), which is hereby incorporated by reference in its entirety.

A variety of suitable host-vector systems may be utilized to express the recombinant peptide mimetic. Primarily, the vector system must be compatible with the host used. Host-vector systems include, without limitation, the following: bacteria transformed with bacteriophage DNA, plasmid DNA, or cosmid DNA; microorganisms such as yeast containing yeast vectors; mammalian cell systems infected with virus (e.g., vaccinia virus, adenovirus, etc.); insect cell systems infected with virus (e.g., baculovirus); and plant cells infected by bacteria.

Purified peptides may be obtained by several methods readily known in the art, including ion exchange chromatography, hydrophobic interaction chromatography, affinity chromatography, gel filtration, and reverse phase chromatography. The peptide is preferably produced in purified form (preferably at least about 80 % or 85 % pure, more preferably at least about 90 % or 95 % pure) by conventional techniques. Depending on whether the recombinant host cell is made to secrete the peptide into growth medium (see U.S. Pat. No. 6,596,509 to Bauer et al., which is hereby incorporated by reference in its entirety), the peptide can be isolated and purified by centrifugation (to separate cellular components from supernatant containing the secreted peptide) followed by sequential ammonium sulfate precipitation of the supernatant. The fraction containing the peptide is subjected to gel filtration in an appropriately sized dextran or polyacrylamide column to separate the peptides from other proteins. If necessary, the peptide fraction may be further purified by HPLC.

A second aspect of the present invention relates to a wound healing composition that comprises one or more of the recombinant fibronectin peptide mimetics of the present invention and a synthetic material. Preferably, the recombinant fibronectin peptide mimetic is dispersed throughout the synthetic material. In one embodiment of the present invention, the recombinant fibronectin peptide mimetic is dispersed throughout the synthetic material in a homogenous manner. In another embodiment of the present invention, the recombinant fibronectin peptide mimetic is spatially patterned throughout the synthetic material. In accordance with this aspect of the invention, the synthetic material can be a biocompatible polymer, a biological dermal substitute, or a tissue scaffold.

When used in these wound healing compositions of the present invention, the recombinant fibronectin peptide mimetic can be present in any amount suitable to induce wound healing. In certain embodiments, the peptide can be delivered in a range of 25 nM to 25 mM, more preferably, in a range of 104 μM to 1 mM. The optimal peptide mimetic concentration for treatment will vary depending on the application (e.g., type of wound or tissue regeneration); however, determining the optimal peptide mimetic concentration can be carried out using techniques known to one of skill in the art. Ideally, the lowest effective dose of peptide mimetic that can achieve the desired wound healing or tissue regeneration is administered.

As used herein, a biocompatible polymer refers to a compound that is biostable, bioerodable, and/or bioresorbable. A biocompatible polymer may be a homopolymer or a copolymer and may contain a reactive chemical functionality that allows for grafting. A biocompatible copolymer may contain both hydrophobic and hydrophilic portions and may be a synthetic polymer, derived from naturally occurring polymers, e.g., cellulose, collagen, gelatin, fibrin, chitosan, etc.

In one embodiment of the present invention, the biocompatible polymer comprises a biostable polymer selected from the group consisting of polyurethanes, isobutylene, polystyrene-isobutylene-polystyrene, silicone, a thermoplastic elastomer, an ethylene vinyl acetate copolymer, a polyolefin elastomer, EPDM ethylene-propylene terpolymer rubber, polyamide elastomer, hydrogel, and combinations thereof. Alternatively, the biocompatible polymer comprises a bioerodable or bioresorable polymer selected from the group consisting of polyglycolide, polylactide, poly(lactide-co-glycolide), polycaprolactone, polybutylene succinate, poly(p-dioxanone), polytrimethylene carbonate, polyphosphazenes, specific polyester polyurethanes, polyether polyurethanes, polyamides, polyorthoesters, polyester amides, maleic anhydride copolymers, poly(sebacic anhydride), polyvinyl alcohol, biopolymers, gelatin, glutens, cellulose, starches, chitin, chitosan, alginates, bacterial polymers, poly(hydroxybutyrate), poly(hydroxybutyrate-co-valerate), functionalized polymers, copolymers, and combinations or blends thereof. Other suitable biocompatible polymers include those disclosed in U.S. Pat. No. 7,709,439 to Helmus et al., which is hereby incorporated by reference in its entirety.

As used herein, biological dermal substitute refers to a skin substitute or artificial dermal replacement. The dermal substitute comprises a scaffold into which cells can migrate and repair a wound. Several biological dermal substitutes are known in the art, including, without limitation, acellular dermal substitute (ADM), a dermal collagen matrix derived from banked human skin that has been treated to remove all cellular component (see Takami et al., “Dispase/Detergent Treated Dermal Matrix as a Dermal Substitute,” Burns 22:182-90 (1996), which is hereby incorporated by reference in its entirety; Alloderm® (LifeCell Corporation, Branchburg, N.J.), also a dermal collagen matrix derived from banked human skin that is treated to remove most cellular components; Dermagraft TC® (Advanced Tissue Sciences, La Jolla, Calif.), a woven bioabsorable polymer membrane within which human dermal fibroblasts are grown and devitalized; Dermalogen (Collagenesis, Beverely, Mass.), a powdered human dermal collagen matrix that is treated to remove some cellular components; Integra® (Integra Life Sciences Corp., Plainsboro, N.J.), a bilayer artificial skin replacement with a dermal layer composed of bovine collagen gel cross-linked with shark chondroitin-6-sulfate. Other biological dermal substitutes known in the art are suitable for use in the present invention.

As used herein, a tissue-scaffold refers to an engineered biomaterial, typically a degradable biomaterial, comprising cells or tissue. Preferred tissue-scaffolds include three-dimensional engineered tissue constructs or organs as described in WO10/135044 to Dalecki et al., which is hereby incorporated by reference in its entirety. These constructs comprise a mass of living tissue produced primarily by growth in vitro and share critical structural and functional characteristics with intact tissue, such as distinctive multicellular organization and oriented contractile function. Suitable engineered tissue constructs include muscular constructs, vascular constructs, cartilaginous constructs, skeletal constructs, filamentous/ligament constructs, bone constructs, and skin constructs.

The wound healing composition of the present invention may further comprise one or more additional recombinant proteins or peptides involved in wound healing. The one or more additional recombinant proteins or peptides can be extracellular matrix proteins, growth factors, cytokines, and chemokines, or any combination thereof. The additional agents can be administered in any suitable dosage that is effective to induce or to enhance the desired wound healing. Preferably, the lowest effective dose that can contribute to the desired wound healing is utilized. Suitable extracellular matrix proteins include, without limitation, glycosaminoglycan, a proteoglycan, collage, elastin, laminin, alginate, a chitin derivative, fibrin, fibrinogen, and any combination thereof. Suitable growth factors include, without limitation, platelet derived growth factor (PDGF), tumor necrosis factor-alpha (TNF-α), TNF-β, epidermal growth factor (EGF), keratinocyte growth factor, vascular endothelial growth factors (VEGFs), fibroblast growth factors (FGFs), tumor necrosis factor, insulin growth factor (IGF), and any combination thereof.

In a preferred embodiment of the present invention, the one or more additional recombinant proteins or peptides are spatially patterned throughout the synthetic material to facilitate the wound healing process. For example, pro-migratory proteins are patterned to contact the outside edge of the wound while pro-growth proteins are patterned to contact the center of the wound.

The wound healing composition of the present invention may also include other wound healing agents, such as anti-inflammatory agents, antimicrobial agents, healing promoters, and combinations thereof.

Anti-inflammatory agents useful for dispersion in the wound healing composition of the present invention include, without limitation, analgesics (e.g., NSAIDS and salicyclates), hormones (glucocorticoids), and skin and mucous membrane agents. Specifically, the anti-inflammatory agent can include dexamethasone. Alternatively, the anti-inflammatory agent can include sirolimus (rapamycin), which is a triene macrolide antibiotic isolated from Steptomyces hygroscopicus. The anti-inflammatory agents can be administered in any suitable dosage that is effective to induce or to enhance the desired wound healing. Preferably, the lowest effective dose that can contribute to the desired wound healing is utilized.

A variety of antibiotics and antimicrobials can also be dispersed in the wound healing compositions to indirectly promote natural healing processes by preventing or controlling infection. Suitable antibiotics include aminoglycoside antibiotics (e.g., gentamycin, tobramycin), quinolones, beta-lactams (e.g., ampicillin, cefalosporines), ciprofloxacin, erythromycin, vancomycin, oxacillin, cloxacillin, methicillin, lincomycin, and colistin. Suitable antimicrobials include, for example, Adriamycin PFS/RDF® (Pharmacia and Upjohn), Blenoxane® (Bristol-Myers Squibb Oncology/Immunology), Cerubidine®. (Bedford), Cosmegen® (Merck), DaunoXome® (NeXstar), Doxil® (Sequus), Doxorubicin Hydrochloride® (Astra), Idamycin® PFS (Pharmacia and Upjohn), Mithracin® (Bayer), Miamycin®. (Bristol-Myers Squibb Oncology/Immunology), Nipen® (SuperGen), Novantrone® (Immunex) and Rubex® (Bristol-Myers Squibb Oncology/Immunology). The antibiotics and antimicrobial agents can be administered in any suitable dosage that is effective to induce or to enhance the desired wound healing. Preferably, the lowest effective dose that can contribute to the desired wound healing is utilized.

Suitable wound healing promoters include, without limitation, vitamin A and synthetic inhibitors of lipid peroxidation. Other suitable wound healing promoters include agents that promote natural wound healing processes by endothelial cells. These wound healing agents include any bioactive agent that donates, transfers, or releases nitric oxide, elevates endogenous levels of nitric oxide, stimulates endogenous synthesis of nitric oxide, or serves as a substrate for nitric oxide synthase or that inhibits proliferation of smooth muscle cells. Such wound-healing agents include, for example, aminoxyls, furoxans, nitrosothiols, nitrates and anthocyanins; nucleosides, such as adenosine; nucleotides, such as adenosine diphosphate (ADP) and adenosine triphosphate (ATP); histamine and catecholamines; lipid molecules, such as sphingosine-1-phosphate and lysophosphatidic acid; amino acids, such as arginine and lysine; peptides such as the bradykinins, substance P and calcium gene-related peptide (CGRP), and proteins, such as insulin, vascular endothelial growth factor (VEGF), and thrombin. The wound healing promoting agents can be administered in any suitable dosage that is effective to induce or to enhance the desired wound healing. Preferably, the lowest effective dose that can contribute to the desired wound healing is utilized.

These wound healing compositions of the present invention are suitable for administeration to mammals for veterinary use, such as with domestic animals, and clinical use in humans in a manner similar to other therapeutic agents. In general, the dosage required for therapeutic efficacy will vary according to the type of use and mode of administration, as well as the particularized requirements of individual hosts.

Such compositions are typically prepared as liquid solutions or suspensions, or in solid forms. Formulations for wound healing usually will include such normally employed additives such as binders, fillers, carriers, preservatives, stabilizing agents, emulsifiers, buffers and excipients as, for example, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, cellulose, magnesium carbonate, and the like. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations, or powders, and typically contain 1%-95 % of active ingredient, preferably 2%-70%.

The compositions are also prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection may also be prepared.

The wound healing compositions of the present invention are often mixed with diluents or excipients which are physiological tolerable and compatible. Suitable diluents and excipients are, for example, water, saline, dextrose, glycerol, or the like, and combinations thereof. In addition, if desired the compositions may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, stabilizing or pH buffering agents.

Additional formulations which are suitable for other modes of administration, such as topical administration, include salves, tinctures, creams, lotions, gels, ointments, and, in some cases, suppositories. For salves and creams, traditional binders, carriers and excipients may include, for example, polyalkylene glycols or triglycerides.

Another aspect of the present invention relates to a wound dressing that comprises the wound healing composition or recombinant peptide of the present invention, described supra, and a wound dressing material.

The wound dressing material can be any material applied to a wound for protection, absorbance, drainage, etc. Numerous types of dressings are commercially available, including films (e.g., polyurethane films), hydrocolloids (hydrophilic colloidal particles bound to polyurethane foam), hydrogels (cross-linked polymers containing about at least 60 % water), foams (hydrophilic or hydrophobic), calcium alginates (nonwoven composites of fibers from calcium alginate), cellophane (cellulose with a plasticizer), gauze, alginate, polysaccharide paste, granules, and beads.

Another aspect of the present invention relates to a method of treating a wound. This method involves providing the wound healing composition of the present invention and applying the wound healing composition to the wound under conditions suitable to promote healing of the wound. In a preferred embodiment of the present invention, the wound healing composition enhances or increases the rate of healing of the wound being treated.

In accordance with this aspect of the present invention, the wound healing composition of the present invention is administered in a suitable dosage that is effective to induce or to enhance the desired wound healing. Preferably, the lowest effective dose that can contribute to the desired wound healing is utilized. The wound healing composition of the present invention is preferably reapplied periodically until the wound heals. For example, the wound healing composition may be applied twice daily, daily, every other day, of every two days, until the desired healing is achieved (e.g., 50-70 % wound closure). The optimal dosage and frequency of application will vary depending on the wound and can be determined using techniques readily known to one of skill in the art.

In one embodiment of the present invention, the wound healing composition comprises a biocompatible polymer. Once the polymer based composition is contacted with the wound it is allowed to polymerize, thereby increasing the rate of healing.

The wound healing composition of the present invention is suitable for treatment of internal and external wounds. The wound healing composition of the present invention is particularly suitable for treatment of chronic non-healing wounds, such as diabetic ulcers, pressure ulcers, leg ulcers, dermal ulcers, burns, corneal wounds, and incisions which involve body tissues being cut, abraded, or otherwise damages.

In another embodiment of the invention, the wound healing composition of the present invention is used for inducing or enhancing the regeneration of healthy tissue (e.g., cartilage, bone, nervous tissue, muscle tissue, soft tissue, vasculature, etc.). Treatment with the wound healing composition of the present invention is particularly suitable for conditions that cause organ damage, such as, e.g., liver disease (cirrhosis), pancreatic disease, and lung disease (emphysema). Alternatively, the wound healing composition of the present invention is useful for regenerating healthy tissue after reconstructive or elective plastic surgery.

EXAMPLES

The following examples are provided to illustrate embodiments of the present invention but they are by no means intended to limit its scope.

Materials and Methods for Examples 1-6

Reagents, antibodies, and cells. Human plasma fibronectin was isolated from Cohn's fraction I and II (Miekka et al., “Rapid Methods for Isolation of Human Plasma Fibronectin,” Thromb. Res. 27:1-14 (1982), which is hereby incorporated by reference in its entirety). Type I collagen was extracted from rat tail tendons using acetic acid and precipitated with NaCl (Windsor et al., MATRIX METALLOPROTEINASES 10.8.6-10.8.7 (Wiley & Sons, Inc. 2002), which is hereby incorporated by reference in its entirety). Human fibrinogen was a gift from Dr. Patricia Simpson-Haidaris (University of Rochester, Rochester, N.Y.). Recombinant vitronectin was expressed and purified as previously described (Wojciechowski et al., “Expression, Production, and Characterization of Full-Length Vitronectin in Escherichia coli,” Prot. Expr. Pur 36(1):131-138 (2004), which is hereby incorporated by reference in its entirety). GRGDSP (SEQ ID NO: 24) peptides were obtained from Sigma (St. Louis, Mo.). FN12-8 monoclonal antibody was obtained from Takara (Madison, Wis.); horseradish peroxidase-conjugated goat anti-mouse antibody was from Bio-Rad (Hercules, Calif.). Tissue culture supplies were from Corning/Costar (Cambridge, Mass.). Unless otherwise indicated, chemical reagents were from J. T. Baker (Phillipsburg, N.J.) or Sigma.

Mouse embryonic fibronectin—null fibroblasts (FN-null MEFs; provided by Dr. Jane Sottile, University of Rochester, Rochester, N.Y.) were cultured on collagen I-coated dishes under fibronectin- and serum-free conditions using a 1:1 mixture of CELLGRO® (Mediatech, Herndon, Va.) and Aim V (Invitrogen) (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998), which is hereby incorporated by reference in its entirety).

Recombinant protein production and purification. A schematic of the recombinant proteins used in this study is shown in FIG. 1A. As noted above, reference to amino acid residues of the fibronectin peptides and domains in the Examples reflects the mature fibronectin protein that does not contain the 31 amino acid leader sequence.

Recombinant GST/III1H,8-10 (Peptide #1 of FIG. 1A), GST/III1H (Peptide #7 of FIG. 1A), GST/III8-10 (Peptide #10 of FIG. 1A), and GST/III8-10,13 (Peptide #11) were produced in E. coli and purified as described (Gui et al., “Identification of the Heparin-Binding Determinants Within Fibronectin Repeat III1: Role in Cell Spreading and Growth,” J. Biol. Chem. 281(46):34816-34825 (2006) and Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which are hereby incorporated by reference in their entirety). A fibronectin fragment in which a C-terminal fragment of Extra domain-B (ED_(B)-C) was coupled to the integrin-binding modules, III8-10 (GST/IIIED_(B)-C,8-10) (Peptide #9 of FIG. 1A), was produced using the sense primer: 5′-CCCAGATCTCTGAGGTGGACCCCGCTAAAC-3′ (SEQ ID NO:25) and antisense primer: 5′-CCCCCCGGGCTATGTTCGGTAATTAATGGAAATTG-3′ (SmaI site in bold; SEQ ID NO:26). The human fibronectin cDNA construct pCEF103 was used as a template (Dufour et al., “Generation of Full-Length cDNA Recombinant Vectors for the Transient Expression of Human Fibronectin in Mammalian Cell Lines,” Exp. Cell Res. 193(2):331-338 (1991), which is hereby incorporated by reference in its entirety). GST/III1H,8-10ΔRRK (R⁶¹³T, R⁶¹⁵T, K⁶¹⁷A) was produced with the forward primer 5′-CCCGGTACCATCCAGTGGAATGCACCACAGCCATCTCACATTTCCAAGTACATTC TCACGTGGACACCTGCAAATTCTGTAGGC-3′ (SEQ ID NO:27). The Kpn1 site is shown in bold and the mutant codons are underlined. The reverse primer was 5′-CCCGAATTCCTATGTGCTGGTGCTGGTGGTG-3′ (SEQ ID NO:28) with the EcoR1 site in bold. GST/III1H,8-10ΔEGQ (E⁶⁴⁷D,Q⁶⁴⁹N) was produced using the following mutant sense primer: 5′-GGTATACGACGGCAACCTGATCAGCATCCAGCACTACG-3′ (SEQ ID NO:29). Mutations are underlined; a BstZ17I site is shown in bold. The antisense primer for GST/III1H,8-10ΔEGQ was the same as that used for GST/III1H,8-10 (5′-CCCCCCGGGCTATGTTCGGTAATTAATGGAAATTG-3′ (SEQ ID NO:30)), which contains a Sma1 site (bold). Human full-length fibronectin cDNA pFH100 was used as a template.

Recombinant fibronectins that contained deletions to type III modules within the cell binding domain were made using GST/III1H,8-10 plasmid DNA as the template. The sense primer, beginning in FNIII1, for these constructs was: 5′-CCCGGATCCATCCAGTGGAATGCACCACAG-3′ (SEQ ID NO:31). The BamH1 site is shown in bold. GST/III1H,8 (Peptide #5 of FIG. 1A) was made with the antisense primer: 5′-GTCACGATCAATTCCCGGGCTATGTTTTCTGTCTTCCTCTA-3′ (SEQ ID NO:32), which contains a Sma1 site shown in bold. GST/III1H,8,10 (Peptide #2 of FIG. 1A) was made with the following antisense primer that includes the 5′ end of FNIII10 and the 3′ end of FNIII8: 5′-GGTCCCTCGGAACATCAGAAACTGTTTTCTGTCTTCCTCTAAGAGG-3′ (SEQ ID NO:33). An AlwNI site is shown in bold. GST/III1H,10 (Peptide #4 of FIG. 1A) was made using the antisense primer: 5′-CCAGGTCCCTCGGAACATCAGAAACTGTGCTGGTGCTGGTGG-3′ (SEQ ID NO:34), which runs from the PpuMI site in FNIII10 (bold) into the 3′ end of FNIII1-H. GST/III1H,9-10 (Peptide #3) was made by first engineering a ClaI site (bold) into FNIII1H of pGEX-2T/III1H,8-10 with the sense primer: 5′-GGTATACGAGGGCCAGCTCATATCGATCCAGCAGTACGG-3′ (SEQ ID NO:35). The BstZ17I site in FNIII1 is underlined. FNIII1H was then coupled directly to FNIII9 by deleting FNIII8 from pGEX2T/III1H,8-10 with the sense primer: 5′-CATATCGATCCAGCAGTACGGCCACCAAGAAGTGACTCGCTTTGACTTCACCAC CACCAGCACCAGCACAGGTCTTGATTCCCCAACTGG-3′ (SEQ ID NO:36). The Cla1 site, shown in bold, was used to move this fragment into pGEX-2T/III1H,8-10.

The RGD chimera, GST/III1H,8^(RGD) (Peptide #6 of FIG. 1A), was produced using the following mutant sense primer: 5′-GTGAGTGTCTCCAGTGTCTACGGCCGTGGAGACTCGCCGGCAAGCAGCACACCTC TTAGAGGAAGACAGAAAACATAGGAATTCA-3′ (SEQ ID NO:37). The insert from FNIII10 (bases 4487-4510 in pFH100; underlined), which encodes for the GRGDSPAS sequence (SEQ ID NO: 38), was inserted between base 3946 and base 3959 (Y¹⁴⁰² and S¹⁴⁰⁷) of FNIII8 (pFH100), leading to the addition of four amino acids (RGDS) to FNIII8. The EcoR1 site is shown in bold. The FNIII10 insert contains an engineered NgoMIV site as a marker. The antisense primer for GST/III1H,8^(RGD) (5′-GGTATACGAGGGCCAGCTCATATCGATTCAGCAGTACGGCC-3′ (SEQ ID NO:39)) contains a BstZ17I site shown in bold. GST/III8^(RGD) (Peptide #8 of FIG. 1A) was engineered using pGEX-2T/III1H,8^(RGD) as a template. The sense primer used was: 5′-CGGATCCGCTGTTCCTCCTCCCACTGACCTGCG-3′(SEQ ID NO:40), with the BamHI site shown in bold. The antisense primer for GST/III8^(RGD) (5′-CGAATTCCTATGTTTTCTGTCTTCC-3′ (SEQ ID NO:41)) contains an EcoRI site shown in bold. For all protein constructs, PCR-amplified DNA was cloned into pGEX-2T (Amersham Biosciences) and transfected into DH5α bacteria (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety). DNA was sequenced to confirm the presence of the mutations. GST-tagged fibronectin constructs were isolated on glutathione-Sepharose (Amersham Biosciences) and dialyzed extensively against PBS (Hocking et al., “Fibronectin's III-1 Module Contains a Conformation-Dependent Binding Site for the Amino-Terminal Region of Fibronectin,” J. Biol. Chem. 269:19183-19191 (1994), which is hereby incorporated by reference in its entirety). Proteins were filter-sterilized and purity was assessed by SDS-polyacrylamide gel electrophoresis (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety) (FIG. 1B). Purified proteins were stored in aliquots at −80° C.

Cell adhesion and proliferation assays. Tissue culture plates (48- or 96-well) were coated with recombinant fibronectin proteins or full-length ECM proteins diluted in PBS at the indicated concentrations for 90 min at 37° C. Unbound protein was removed and wells were washed with PBS. For cell proliferation assays, FN-null MEFs were seeded at 2.5×10³ cells/cm² in Aim V/Cellgro and incubated for 4 days at 37° C., 8 % CO₂. For cell adhesion assays, FN-null MEFs were seeded at 1.5×10⁵ cells/cm² in Aim V/Cellgro and cells were allowed to adhere for 30 min at 37° C., 8 % CO₂. After incubation, cells were washed with PBS and fixed with 1 % paraformaldehyde. Cells were stained with 0.5 % crystal violet, solubilized in 1 % sodium dodecyl sulfate (SDS), and the absorbance at 590 nm was measured with a microplate spectrophotometer (Bio-Rad) (Hocking et al., “Activation of Distinct α₅β₁-Mediated Signaling Pathways by Fibronectin's Cell Adhesion and Matrix Assembly Domains,” J. Cell Biol. 141:241-253 (1998)).

Solid-phase enzyme linked immunosorbent assay. Tissue culture plates (96-well) were incubated with recombinant fibronectin proteins or plasma fibronectin diluted in PBS at the indicated concentrations for 90 min at 37° C. Wells were washed with PBS to remove unbound protein, then blocked with 1% BSA in PBS. Bound proteins were detected using an anti-FNIII10 monoclonal antibody (FN12-8, 1 μg/ml) followed by horseradish peroxidase-conjugated goat anti-mouse secondary antibodies. Wells were washed with PBS and the assay was developed using 2,2-azino-bis(3-ethylbenzthiazolinesulfonic acid) and the absorbance at 405 nm was measured.

Cell migration assay. An in vitro wound repair assay was used to measure cell migration (Hocking et al., “Fibronectin Polymerization Regulates Small Airway Epithelial Cell Migration,” Am. J. Physiol. Lung Cell Mol. Physiol. 285:L169-L179 (2003), which is hereby incorporated by reference in its entirety). Tissue culture plates (35-mm) were coated with recombinant fibronectin constructs or full-length fibronectin at 200 nM in PBS for 90 min at 37° C. FN-null MEFs were seeded at 7.4×10⁴ cells/cm² in Aim V/Cellgro. Cells were allowed to adhere and spread for either 4 or 16 h to establish a confluent monolayer. A thin section of the monolayer was carefully removed with a sterile, plastic microspatula. Cells were washed twice with Aim V/Cellgro. Five non-overlapping regions of the wound were viewed immediately after wounding with an Olympus inverted microscope using a 4× objective (time=0 h). Phase contrast images of each region were obtained using a Spot digital camera (Diagnostic Instruments, Sterling Heights, Mich.). Images were obtained of the five non-overlapping regions at various times after wounding. A numbered grid was marked on the bottom of the tissue culture plates prior to cell seeding to ensure that the same regions were being photographed at each time point. The average width of the initial wound was ˜500 μm. Wound area measurements were obtained using ImagePro-Plus software (Media Cybernetics, Silver Spring, Md.). Cell migration was calculated as original cleared area (time=0 h)−cleared area (time=2, 4, 6, or 8 h).

Collagen gel contraction assay. Collagen gel contraction assays were performed as described previously (Hocking et al., “Stimulation of Integrin-Mediated Cell Contractility by Fibronectin Polymerization,” J. Biol. Chem. 275:10673-10682 (2000), which is hereby incorporated by reference in its entirety). Neutralized collagen gels were prepared by mixing collagen type I with 1× Dulbecco's modified Eagle's medium (DMEM; Life Technologies), 2× concentrated DMEM, and 0.1 NaOH on ice for final concentrations of 0.8 mg/ml collagen and 1×DMEM, pH 7.2. FN-null MEFs were added to the collagen mixture to a final concentration of 2×10⁵ cells/ml. An equal volume of Aim V/Cellgro was added to aliquots of the collagen mixture for ‘no cell’ controls. Recombinant fibronectin proteins or plasma fibronectin were added to the collagen/cell mixtures at various concentrations. Aliquots (0.1 ml) of the collagen/cell mixture were added to wells of tissue culture plates (96-well) precoated with 2% BSA in PBS. Gels were allowed to polymerize for 1 h at 37° C., 8% CO₂. To form floating gels, DMEM (0.1 ml/well) was added and wells were scored with a pipette tip. Following a 20 h incubation at 37° C., 8% CO₂, gels were removed from their wells and weighed (Model AE260, Mettler, Toledo, Ohio). Volumetric collagen gel contraction was calculated as the decrease in gel weight relative to the control, no-cell gel weight.

Statistical analysis. Data are presented as mean±standard error of the mean (SEM) and represent one of at least three experiments performed in either triplicate or quadruplicate. Statistical comparisons were performed using one-way analysis of variance (ANOVA) followed by Tukey's post-test, with GraphPad Prism Version 4 software (LaJolla, Calif.). Differences were considered significant for p values less than 0.05.

Example 1 GST/II1H,8-10 Supports Cell Adhesion and Spreading, and Enhances Cell Proliferation

A recombinant fibronectin construct (GST/III1H,8-10) was previously developed that mimics many of the cellular effects of ECM fibronectin, by directly coupling the cryptic, heparin-binding fragment of the first type III repeat of fibronectin to the integrin-binding domain (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety). Addition of soluble GST/III1H,8-10 to the culture media of adherent FN-null MEFs enhances cell spreading, growth, and contractility (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety), increases the migration rate of small airway epithelial cells (Hocking et al., “Fibronectin Polymerization Regulates Small Airway Epithelial Cell Migration,” Am. J. Physiol. Lung Cell Mol. Physiol. 285:L169-L179 (2003), which is hereby incorporated by reference in its entirety), and induces local arteriolar vasodilation in vivo (Hocking et al., “Extracellular Matrix Fibronectin Mechanically Couples Skeletal Muscle Contraction with Local Vasodilation,” Circ. Res. 102:372-379 (2008), which is hereby incorporated by reference in its entirety). To develop fibronectin matrix mimetics as functional ligands for adhesive biomaterials, studies were conducted to characterize the proliferative response of FN-null MEFs cells to immobilized GST/III1H,8-10. The use of FN-null MEFs allows the characterization of cell behavior in response to the recombinant fibronectin proteins in the absence of endogenous full-length fibronectin and the identification of specific effects of individual domains and amino acid sequences of fibronectin on cell function. Cells were seeded at low density onto tissue culture plates coated with various recombinant fibronectin fragments and cell number was determined after 4 days. The extent of cell proliferation on GST/III1H,8-10-coated substrates was compared to that observed in response to substrates coated with the following ligands: (i) an integrin-binding fragment lacking FNIII1H (GST/III8-10) (Peptide #10, FIG. 1A), (ii) a construct in which the carboxyl-terminal heparin-binding domain of fibronectin was coupled to FNIII8-10 (GST/III8-10,13) (Peptide #11, FIG. 1A), and (iii) plasma fibronectin. At 24 hours after seeding, cells adherent to the fusion protein substrates were well-spread and displayed morphologies similar to that observed with cells adherent to plasma fibronectin (FIG. 2A, top row). Cells proliferated over the 4 day period on all substrates tested and formed a near-confluent monolayer on substrates coated with GST/III1H,8-10 (FIG. 2A, bottom row, first panel). Relative cell number on Day 4 was quantified as a function of protein coating concentration. Cell number on surfaces pre-coated with either 200 nM or 400 nM GST/III1H,8-10 was significantly greater than that observed on surfaces pre-coated with either plasma fibronectin or the integrin-binding fragment, GST/III8-10 (FIG. 2B). Average cell numbers obtained from surfaces pre-coated with GST/III1H,8-10 at 200 nM were 1.32±0.08 (n=5) and 1.49±0.05 (n=15)-fold greater than those obtained on surfaces coated with the same molar concentration of plasma fibronectin or GST/III8-10, respectively. The increase in cell number observed on GST/III1H,8-10-coated surfaces required FNIII1H, as cell number on GST/III8-10,13-coated surfaces was similar to GST/III8-10-coated surfaces (FIG. 2B).

To compare ligand densities of the substrates, ELISAs were performed on tissue culture plates coated with increasing concentrations of protein. At protein coating concentrations less than 200 nM, differences in the relative amount of protein bound to the tissue culture plastic were observed, with GST/III8-10 and plasma fibronectin binding more efficiently than either GST/III1H,8-10 or GST/III8-10,13 (FIG. 3A). For all fusion proteins tested, ligand surface density reached saturation at a concentration of 200 nM. No differences in ligand density were observed among the various recombinant fusion proteins at coating concentrations of 200 nM and 400 nM (FIG. 3A). The ligand density of plates coated with plasma fibronectin at 400 nM was slightly greater than that observed with the recombinant proteins (FIG. 3A). Together, these data indicate that the increase in cell number observed on substrates coated with GST/III1H,8-10 (FIG. 2B) was not due to differences in the coating density of the proteins.

To quantify cell attachment to the various proteins, adhesion assays were performed 30 min after seeding cells at high density onto tissue culture plates pre-coated with increasing concentrations of protein. No differences in cell number were detected among the various groups at coating concentrations greater than 50 nM (FIG. 3B), indicating that the differences in cell number observed after 96 h were not due to differences in initial cell adhesion. As expected, cells did not adhere to wells coated with GST alone (FIG. 3B). Taken together, these data indicate that surfaces coated with GST/III1H,8-10 support cell adhesion and spreading and promote cell proliferation to a greater extent than surfaces coated with either plasma fibronectin or fragments with only integrin-binding activity.

Example 2 The Heparin-Binding Site in FNIII1H is Essential but not Sufficient for Increased Cell Growth

To further evaluate the role of FNIII1H in the proliferative response to GST/III1H,8-10, a fusion protein was produced in which the analogous C-terminal region of the ED-B module of fibronectin was substituted for FNIII1H (GST/IIIED_(B)-C,8-10) (Peptide #9, FIG. 1A). FN-null MEFs were seeded onto surfaces coated with 200 nM GST/III1H,8-10, GST/IIIED_(B)-C,8-10, GST/III8-10, or GST/III1H and cell number was determined after 96 h. Similar to results shown in FIG. 2B, surfaces coated with GST/III1H,8-10 produced a significant increase in cell number versus surfaces coated with either GST/III8-10 or GST/IIIED_(B)-C,8-10 (FIG. 4A). No difference in initial cell adhesion to surfaces coated with GST/III1H,8-10, GST/III8-10, or GST/IIIED_(B)-C,8-10 were observed (FIG. 4B). Surfaces coated with GST/III1H alone did not support either cell adhesion (FIG. 4B) or proliferation (FIG. 4A).

The growth-promoting site in soluble GST/III1H,8-10 was recently localized to the heparin-binding sequence, Arg⁶¹³-Trp⁶¹⁴-Arg⁶¹⁵-Pro⁶¹⁶-Lys⁶¹⁷, in FNIII1 (corresponding to amino acid residues 644-648 of SEQ ID NO:1). To further localize the growth-stimulating site in FNIII1H, a construct was produced in which only the charged amino acid sequences within the R⁶¹³WRPK sequence were mutated to non-charged amino acids (R⁶¹³T, R⁶¹⁵T, K⁶¹⁷A; GST/III1H,8-10ΔRRK). An additional control fusion protein was produced in which a separate, highly conserved sequence in FNIII1H, E⁶⁴⁷G⁶⁴⁸Q⁶⁴⁹, was mutated (E⁶⁴⁷D, Q⁶⁴⁹N; GST/III1H,8-10ΔEGQ). FN-null MEFs were seeded onto surfaces coated with 200 nM of the various fusion proteins and cell number was determined after 96 h. Cell number on surfaces coated with GST/III1H,8-10ΔRRK was less than that observed on surfaces coated with GST/III1H,8-10, and was similar to that observed on GST/III8-10,13-coated surfaces (FIG. 4C). Cell number on GST/III1H,8-10ΔEGQ was not different than that observed on GST/III1H,8-10 (FIG. 4C), providing additional evidence that the growth-promoting activity of FNIII1 is specific to Arg⁶¹³, Arg⁶¹⁵, Lys⁶¹⁷ and that differences in cell number were not due to non-specific structural changes in the mutated protein. No differences in initial cell adhesion were observed among the groups (FIG. 4D). Taken together, these results indicate that the Arg⁶¹³_Arg⁶¹⁵_Lys⁶¹⁷ sequence in FNIII1H mediates the enhanced growth response to GST/III1H,8-10, but that in the absence of FNIII8-10, FNIII1H is unable to support cell adhesion.

Example 3 FNIII8 and FNIII10 are Required for the Cell Growth Response

FNIII8, FNIII9, and FNIII10 form the primary integrin-binding region of fibronectin, regulating cell adhesion and cell surface receptor specificity (Magnusson et al., “Fibronectin: Structure, Assembly, and Cardiovascular Implications,” Arterio. Thromb. Vasc. Biol. 18:1363-1370 (1998), which is hereby incorporated by reference in its entirety). FNIII10 contains the integrin-binding, RGD sequence (Pierschbacher et al., “Variants of the Cell Recognition Site of Fibronectin that Retain Attachment-Promoting Activity,” Proc. Natl. Acad. Sci. U.S.A. 81:5985-5988 (1984), which is hereby incorporated by reference in its entirety), whereas FNIII9 contains a sequence, termed the synergy site, which promotes binding to α5β1 integrins (Aota et al., “The Short Amino Acid Sequence Pro-His-Ser-Arg-Asn in Human Fibronectin Enhances Cell-Adhesive Function,” J. Biol. Chem. 269(40):24756-24761 (1994), which is hereby incorporated by reference in its entirety). Thus far, the data indicate that the integrin-binding domain, FNIII8-10, is necessary for adhesion and growth in response to GST/III1H,8-10 (FIG. 4). To determine whether all three integrin-binding modules are necessary for the proliferative response to GST/III1H,8-10, a series of fusion proteins were produced in which one or two modules within the integrin-binding region were deleted. The modules deleted and the constructs produced were: (i) FNIII9 (GST/III1H,8,10) (Peptide #2, FIG. 1A), (ii) FNIII8 (GST/III1H,9-10) (Peptide #3, FIG. 1A), (iii) FNIII8 and FNIII9 (GST/III1H,10) (Peptide #4, FIG. 1A), and (iv) FNIII9 and FNIII10 (GST/III1H,8) (Peptide #5, FIG. 1A). FN-null MEFs were seeded onto surfaces coated with the various fusion proteins and cell number was determined on Day 4. Deleting FNIII9 from GST/III1H,8-10 did not lead to a difference in cell number compared to the original matrix mimetic (GST/III1H,8,10 versus GST/III1H,8-10; FIG. 5A). In contrast, deleting FNIII8 from GST/III1H,8-10 resulted in a reduction in cell number on Day 4 (GST/III1H,9-10 and GST/III1H,10 versus GST/III1H,8-10; FIG. 5A). Cell adhesion to surfaces coated with GST/III1H,8,10, GST/III1H,9-10 or GST/III1H,10 was similar to that observed on GST/III1H,8-10-coated surfaces (FIG. 5B), indicating that the differences in cell number observed on Day 4 were not due to differences in initial cell attachment. Cells did not adhere to the construct lacking FNIII10 (GST/III1H,8; FIG. 5B), indicating that FNIII8 cannot support cell adhesion in the absence of FNIII10. Taken together, these data indicate that GST/III1H,8,10 supports cell adhesion and promotes cell growth to a similar extent as the original construct, GST/III1H,8-10. In addition, FNIII8 and FNIII10, but not FNIII9, are required for the full proliferative response to the fibronectin matrix mimetics.

Example 4 RGD-Chimeras Support Cell Adhesion and Promote Cell Growth

The cell attachment activity of fibronectin can be duplicated by peptides containing the highly conserved, integrin-binding Arg-Gly-Asp (RGD) sequence (Pierschbacher et al., “Variants of the Cell Recognition Site of Fibronectin that Retain Attachment-Promoting Activity,” Proc. Natl. Acad. Sci. U.S.A. 81:5985-5988 (1984), which is hereby incorporated by reference in its entirety). To further refine GST/III1H,8,10 as a fibronectin matrix mimetic, fusion proteins were engineered in which FNIII10 was deleted and instead, the adhesive RGDS sequence was inserted into FNIII8. The RGDS sequence in FNIII10 is located in a unique loop connecting β-strands F and G (Main et al., “The Three-Dimensional Structure of the Tenth Type III Module of Fibronectin: An Insight Into RGD-Mediated Interactions,” Cell 71:671-678 (1992), which is hereby incorporated by reference in its entirety). Therefore, the FNIII10 sequence, Arg-Gly-Asp-Ser-Pro-Ala-Ser (GRGDSPAS) was inserted into the analogous site in FNIII8. Two fusion proteins were produced: (i) GST/III1H,8^(RGD) (Peptide #6, FIG. 1A) and (ii) GST/III8^(RGD) (Peptide #7, FIG. 1A). Cell adhesion assays were conducted to compare cell attachment activities of the RGD chimeras to the original construct, GST/III1H,8-10. Cell adhesion to surfaces coated with GST/III1H,8^(RGD) was similar to that observed on GST/III1H,8-10-coated surfaces at all protein coating concentrations (FIG. 6A). Cells did not adhere to GST/III1H lacking the 8^(RGD) sequence (FIG. 6A). These data indicate that the adhesive activity of FNIII10 can be duplicated by inserting the RGDS-loop into FNIII8.

To assess the RGD-containing chimeras as growth-promoting adhesive substrates, FN-null MEFs were seeded onto wells coated with 200 nM of the various fusion proteins and cell number was determined after 96 h. Surfaces coated with GST/III1H,8^(RGD) supported a similar level of cell growth as did surfaces coated with the original mimetic, GST/III1H,8-10 (FIG. 6B), and was greater than that observed with cells adherent to surfaces coated with RGD peptides alone (FIG. 6B). Of note, after 4 days, cells were no longer adherent to wells coated with GRGDSP peptides (FIG. 6B).

Dose-response studies indicate that the growth-promoting activity of GST/III1H,8^(RGD) was nearly identical to that of GST/III1H,8-10 at various protein coating concentrations (FIG. 7A). Removal of FNIII1H from GST/III1H,8^(RGD) (GST/III8^(RGD)) resulted in significantly lower cell numbers on Day 4 (FIG. 7A), providing further evidence that the heparin-binding fragment of FNIII1 is required for the enhanced cell growth response. No differences in initial cell adhesion were observed on surfaces coated with GST/III8^(RGD), GST/III1H,8-10 and GST/III1H,8^(RGD) (FIG. 7B). Furthermore, a comparison of the proliferative activity of the fibronectin matrix mimetics to that of other intact ECM ligands revealed that surfaces coated with GST/III1H,8^(RGD) promoted cell growth to a similar extent as vitronectin-coated surfaces, and to a greater extent than that observed for fibrinogen- or gelatin-coated surfaces (FIG. 8). Taken together, these data indicate that by inserting the RGD loop into FNIII8, both FNIII9 and FNIII10 can be removed from the initial matrix mimetic without loss of cell adhesion and growth-promoting activity.

Example 5 Recombinant Fibronectin Matrix Mimetics Support Cell Migration

The ability of the recombinant fibronectin constructs to support cell migration was assessed using an in vitro assay of wound repair. FN-null MEFs were seeded at high densities onto surfaces coated with 200 nM of the various fusion proteins and allowed to form confluent monolayers. A region of the monolayer was then removed and migration of cells into the denuded space was quantified. Surfaces coated with either the original matrix mimetic (GST/III1H,8-10) or the integrin-binding fragment of fibronectin (GST/III8-10) promoted cell migration into the denuded area to a greater extent than surfaces coated with intact, plasma fibronectin (FIG. 9A). Substituting the heparin-binding module, FNIII13, for FNIII1H (see Peptide #11, FIG. 1A) decreased the rate of cell migration (GST/III1H,8-10 versus GST/III8-10,13; FIG. 9A), resulting in a rate of migration similar to that of plasma fibronectin-coated surfaces (GST/III8-10,13 versus FN; FIG. 9A).

Similar to results obtained in the growth assays (FIG. 5A), removal of FNIII9 from the original matrix mimetic did not reduce the rate of cell migration, which was similar to that of the integrin-binding fragment, GST/III8-10 (GST/III1H,8,10 versus GST/III8-10, FIG. 9B). The rate of cell migration on surfaces coated with the growth-promoting, chimeric construct, GST/III1H,8^(RGD), was similar to that of plasma fibronectin (FIG. 9B). Removing FNIII8 from GST/III1H,8,10 decreased the rate of cell migration (GST/III1H,10 versus GST/III1H,8,10; FIG. 9C), indicating a possible role for FNIII8 in promoting higher rates of cell migration. These data indicate that as adhesive substrates, the recombinant fibronectin matrix mimetics equal or exceed the ability of plasma fibronectin to promote cell migration.

Example 6 Fibronectin Matrix Mimetics Stimulate Collagen Gel Contraction

Collagen gel contraction assays are utilized as in vitro models of collagen matrix reorganization during wound repair (Grinnell et al., “Reorganization of Hydrated Collagen Lattices by Human Skin Fibroblasts,” J. Cell Sci. 66:51-63 (1984), which is hereby incorporated by reference in its entirety). Previous studies showed that fibronectin matrix polymerization stimulates collagen gel contraction (Hocking et al., “Stimulation of Integrin-Mediated Cell Contractility by Fibronectin Polymerization,” J. Biol. Chem. 275:10673-10682 (2000), which is hereby incorporated by reference in its entirety) and that this activity is mimicked by the original matrix mimetic, GST/III1H,8-10 (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety). To assess the ability of the new fibronectin matrix mimetics to stimulate collagen gel contraction, FN-null MEFs were embedded in collagen gels and the extent of contraction after 20 h was determined. Addition of plasma fibronectin or the original matrix mimetic (GST/III1H,8-10) to FN-null MEFs embedded in floating collagen gels stimulated collagen gel contraction (FIG. 10). Addition of either GST/III1H,8,10 or GST/III1H,8^(RGD) to cell-embedded collagen gels stimulated collagen gel contraction to a similar extent as that observed in response to the original matrix mimetic, GST/III1H,8-10 (FIG. 10). The extent of collagen gel contraction in response to GST/III1H,8,10 and GST/III1H,8^(RGD) was significantly greater than that observed in response to the control protein, GST (FIG. 10).

Discussion of Examples 1-6

Described herein is the development of several recombinant fibronectin proteins that couple the “open” conformation of FNIII1 with integrin-binding sequences in order to mimic the effects of the ECM form of fibronectin on cell growth and migration. The bioactivity of the fibronectin matrix mimetics was compared to full-length, plasma fibronectin and to integrin-binding fragments and peptides. These studies show that a chimeric fibronectin fragment composed of FNIII1H and FNIII8, with the RGDS loop inserted into FNIII8, supports cell adhesion and migration, stimulates collagen gel reorganization, and displays enhanced proliferative activity over integrin-binding fibronectin fragments and other full-length ECM proteins. The growth-promoting activity in FNIII1H was localized to amino acids Arg⁶¹³, Arg⁶¹⁵, and Lys⁶¹⁷, and new evidence demonstrates that FNIII8 has cell growth- and migration-promoting properties.

Surfaces presenting the RGD-loop in FNIII8 exhibited identical adhesive activities compared to the original matrix mimetic (GST/III1H,8-10; FIG. 6A), which was comparable to that observed with integrin-binding fragments (FIG. 3B). Deleting FNIII9 from the original matrix mimetic did not decrease the proliferation response of cells (FIG. 5A) and was not required for cell migration (FIG. 9B), indicating that binding of the PHSRN sequence in FNIII9 to α5β1 integrins (Aota et al., “The Short Amino Acid Sequence Pro-His-Ser-Arg-Asn in Human Fibronectin Enhances Cell-Adhesive Function,” J. Biol. Chem. 269(40):24756-24761 (1994) and Garcia et al., “Distinct Activation States of Alpha5beta1 Integrin Show Differential Binding to RGD and Synergy Domains of Fibronectin,” Biochem. 41(29):9063-9069 (2002), which is hereby incorporated by reference in its entirety) does not contribute to the observed activities. Surfaces coated with the chimeric RGD-construct produced higher levels of cell growth over surfaces coated with linear GRGDSP peptides (FIG. 6B), suggesting that the structural framework of the FNIII module provides support for the RGD loop to allow for higher affinity interactions with integrin receptors (Ruoslahti E, “RGD and Other Recognition Sequences for Integrins,” Annu. Rev. Cell Dev. Biol. 12:697-715 (1996), which is hereby incorporated by reference in its entirety). The growth-promoting activity of the chimeric fibronectin matrix mimetic, GST/III1H,8^(RGD), was comparable to that of the ECM protein, vitronectin, and was greater than that observed for other full-length ECM substrates including fibrinogen and gelatin (FIG. 8). Thus, tethering or incorporating chimeric fibronectin matrix mimetics into biomaterials will provide robust proliferative activity to tissue-engineered scaffolds and medical devices.

The bioactivities of the fibronectin fragments tested were not identical. Surfaces coated with either GST/III1H,8-10 or GST/III1H,8,10 induced high-growth and high-migration responses; GST/III1H,8^(RGD)-coated surfaces provided high-growth and moderate-migration activities; GST/III8-10 induced low-growth but high-migration activities. Hence, engineering interfaces with different fibronectin matrix mimetics and fragments represents a strategy to spatially pattern different cellular responses. In contrast to results obtained in the growth studies, a large decrease in cell migration rate occurred when FNIII10 was removed and replaced by the RGD loop (compare FIG. 6B with FIG. 9B), indicating that an auxiliary site in FNIII10 (Ruoslahti E, “RGD and Other Recognition Sequences for Integrins,” Annu. Rev. Cell Dev. Biol. 12:697-715 (1996), which is hereby incorporated by reference in its entirety) may contribute to enhanced cell migration, but not to enhanced cell growth. On the other hand, deletion of FNIII8 from GST/III1H,8-10 reduced both growth (FIG. 5A) and migration (FIG. 9C). Previous studies have identified a region within the amino-terminus of FNIII8 that is involved in cell adhesion (Aota et al., “Characterization of Regions of Fibronectin Besides the Arginine-Glycine-Aspartic Acid Sequence Required for Adhesive Function of the Cell-Binding Domain Using Site-Directed Mutagenesis,” J. Biol. Chem. 266:15938-15943 (1991), which is hereby incorporated by reference in its entirety). Taken together, the results indicate that at least two additional sites within the cell-binding domain of fibronectin, one in FNIII10 and one in FNIII8, contribute to integrin-mediated cellular responses.

Proteolysis of the first type III repeat of fibronectin at residue Ile⁵⁹⁷ removes both the A and B β strands and results in a carboxyl-terminal fragment that binds to heparin (Litvinovich et al., “Reversible Unfolding of an Isolated Heparin and DNA Binding Fragment, the First Type III Module from Fibronectin,” Biochim. Biophys. Acta. 1119:57-62 (1992), which is hereby incorporated by reference in its entirety). Previous studies localized the growth-promoting activity of GST/III1H,8-10 to the heparin-binding sequence, K⁶¹¹_R⁶_WR_K⁶¹⁹. The preceding Examples herein demonstrate that FNIII1H is also required for the enhanced growth response to surfaces coated with GST/III1H,8-10 and further, pinpoint the growth-enhancing sequence in FNIII1 to R⁶¹³, R⁶¹⁵, and K⁶¹⁷. The cell surface receptor that binds to FNIII1H is currently unknown, however, it is feasible that FNIII1 interacts with cells via heparan sulfate proteoglycans (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes To Lipid Rafts And Stimulates Cell Growth And Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety). Aortic smooth muscle cells adhere to surfaces coated with micromolar concentrations of a similar FNIII1 fragment, III1-C, via a heparin-dependent mechanism that involves α5β1 integrins (Mercurius et al., “Cell Adhesion and Signaling on the Fibronectin 1st Type III Repeat; Requisite Roles for Cell Surface Proteoglycans and Integrins,” BMC Cell Biol. 2:18 (2001), which is hereby incorporated by reference in its entirety). Together, these studies indicate that FNIII1H may bind either directly or indirectly to α5β1 integrins via heparan sulfate proteoglycans to elicit cellular responses. In support of this, it has been shown that FNIII1H must be directly coupled to FNIII8-10 to stimulate cell growth, as individual fragments added simultaneously to cells do not have growth-promoting effects (Hocking et al., “A Cryptic Fragment From Fibronectin's III-1 Module Localizes to Lipid Rafts and Stimulates Cell Growth and Contractility,” J. Cell Biol. 158:175-184 (2002), which is hereby incorporated by reference in its entirety). Similarly, the proliferative response to surfaces coated with a mixture of FNIII1H and FNIII8-10 fragments was not different from that observed with GST/III8-10-coated surfaces.

Fibronectin type III repeats are found in ˜2 % of all human proteins and show a high degree of structural similarity (Bloom et al., “FN3: A New Protein Scaffold Reaches the Clinic,” Drug Discov. Today (19-20):949-955 (2009), which is hereby incorporated by reference in its entirety). The anti-parallel β-sheets of FNIII repeats are composed of three (A, B, and E) and four (C, D, F, and G) β strands that overlap to form a hydrophobic core (Bork et al., “Proposed Acquisition of an Animal Protein Domain by Bacteria,” Proc. Natl. Acad. Sci. U.S.A. 89(19):8990-8994 (1992) and Leahy et al., “Structure of a Fibronectin Type III Domain From Tenascin Phased by MAD Analysis of the Selenomethionyl Protein,” Science 258:987-991 (1992), which are hereby incorporated by reference in their entirety), imparting a high degree of stability to the protein's structure (Litvinovich et al., “Interactions Between Type III Domains in the 110 kDa Cell-Binding Fragment of Fibronectin,” J. Mol. Biol. 248(3):611-626 (1995), which is hereby incorporated by reference in its entirety). The six loops formed at the poles between β strands (termed AB, BC, etc.) are highly variable and can withstand extensive modification without loss of stability (Siggers et al., “Conformational Dynamics in Loop Swap Mutants of Homologous Fibronectin Type III Domains,” Biophys. J. 93(7):2447-2456 (2007) and Billings et al., “Crosstalk Between the Protein Surface and Hydrophobic Core in a Core-Swapped Fibronectin Type III Domain,” J. Mol. Biol. 375(2):560-571 (2008), which are hereby incorporated by reference in their entirety). This inherent stability likely facilitated the insertion of the RGDS sequence into the FG loop of FNIII8. The stability of fibronectin type III repeats has also allowed for the development of FNIII-domains as scaffolds for the display of binding elements (Koide et al., “The Fibronectin Type III Domain as a Scaffold for Novel Binding Proteins,” J. Mol. Biol. 284(4):1141-1151 (1998), which is hereby incorporated by reference in its entirety), while an engineered FNIII scaffold is currently in Phase II trials as an anti-angiogenesis agent (Bloom et al., “FN3: A New Protein Scaffold Reaches the Clinic,” Drug Discov. Today (19-20):949-955 (2009), which is hereby incorporated by reference in its entirety). Both FNIII1 and FNIII8 lack cysteine residues and post-translation modifications (Petersen et al., “Partial Primary Structure of Bovine Plasma Fibronectin: Three Types of Internal Homology,” Proc. Natl. Acad. Sci. U.S.A. 80:137-141 (1983), which is hereby incorporated by reference in its entirety), which facilitates production in bacteria. For the studies described herein, GST/III1H,8^(RGD) was generated with a cleavable GST-tag that allows for rapid purification via glutathione chromatography; yields of ˜4 mg of purified GST/III1H,8^(RGD) per liter of bacterial culture were obtained. The molecular mass of the chimeric matrix mimetic, excluding the GST-tag, is ˜19 kDa. In contrast, the molecular mass of a single, soluble fibronectin molecule is ˜500 kDa. The small size of the fibronectin matrix mimetic decreases potential immunogenicity, provides increased structure and stability over peptides, and reduces the number of binding sites for other receptors.

In conclusion, a small, chimeric fibronectin matrix mimetic has been developed by inserting the integrin-binding RGDS sequence into the FG loop of FNIII8 and then coupling FNIII8^(RGD) to the heparin-binding fragment of FNIII1. Surfaces passively coated with GST/III1H,8^(RGD) support cell adhesion and migration, induce collagen matrix contraction, and display enhanced proliferative activity over either integrin-binding fibronectin fragments or full-length fibronectin. These results provide proof-of-principle for the development of chimeric fibronectin type III repeats as novel adhesive ligands for synthetic biomaterials that support cell migration and stimulate high rates of cell proliferation for wound healing.

Example 7 Fibronectin Matrix Mimetics as Integrin-Specific Adhesive Substrates

As shown supra, fibronectin matrix mimetics, GST/III1H,8-10, GST/III1H,8,10 and GST/III1H,8^(RGD) support cell adhesion, proliferation, and migration to a similar or greater extent than full-length fibronectin. FN-null MEFs were used for these studies as they do not produce endogenous fibronectin and are cultured under fibronectin- and serum-free conditions, thus allowing for direct comparison between fibronectin matrix mimetics and full-length fibronectin. To determine which integrin receptors mediate adhesion to the fibronectin matrix mimetics, various function-blocking anti-integrin antibodies were tested for their ability to block FN-null MEF attachment to protein-coated plates. Blocking antibodies directed against α5, αv, β1, and β3 integrins were used as these integrin subunits are expressed by FN-null MEFs and have been reported to bind full-length fibronectin (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998) and Pankov et al., “Fibronectin at a Glance,” J. Cell Sci. 115(20):3861-3863 (2002), which are hereby incorporated by reference in their entirety). EDTA, a divalent cation chelating agent, was used to inhibit all integrin-mediated adhesion to the substrate. In the presence of α5 or β1 integrin blocking antibodies, cell adhesion to GST/III1H,8-10-coated plates was reduced by 51.0%+/−9.49% and 86.5%+/−3.18%, respectively. In contrast, anti-αv, -β3 or -β5 integrin antibodies had no effect on cell adhesion to GST/III1H,8-10 indicating that α5β1 integrins mediate adhesion to this substrate (FIG. 11A). Cell adhesion to GST/III1H,8,10, which lacks FNIII9 and the α5β1 integrin-binding synergy site, was reduced with α5 (by 28.8%+/−10.9%), αv (49.8%+/−7.84%), β1 (71.0%+/−6.26%) and β3 (30.5%+/−10.7%) integrin-blocking antibodies (FIG. 11B), indicating that cell adhesion to this construct is mediated through a combination of α5β1, αvβ3 and potentially αvβ1 integrins. Cell adhesion to GST/III1H,8^(RGD) was inhibited using either αv or β3 integrin blocking antibodies, by 82.7%+/−7.05% and 85.24%+/−6.09%, respectively (FIG. 11C). In contrast, addition of anti-α5 or β1 integrin antibodies had no effect on cell adhesion to GST/III1H,8^(RGD), indicating that αvβ3 integrins mediate adhesion to GST/III1H,8^(RGD) (FIG. 11C). In comparison, cell adhesion to full-length fibronectin was reduced only with α5 (by 53.0%+/−11.5%) and β1 (by 71.3%+/−3.97%) integrin-blocking antibodies, indicating α5β1 integrin-mediated adhesion to the fibronectin substrate (FIG. 1D). Thus, cell adhesion to both full-length fibronectin and the fibronectin matrix mimetic that has the full cell-binding domain (GST/III1H,8-10) is mediated by α5β1 integrins. Removal of FNIII9 (GST/III1H,8,10) results in cell adhesion via a combination of α5β1 and αvβ3 integrins. Further reducing the cell-binding domain by removing FNIII10 and inserting the GRGDSP loop into FNIII8 (GST/III1H,8^(RGD)) results in cell adhesion that is mediated exclusively by αvβ3 integrins.

Example 8 Fibronectin Matrix Assembly by Cells Adherent to Matrix Mimetics

Previous studies have shown that various adhesive substrates can either support or inhibit cell-dependent assembly of a fibronectin matrix (Bae et al., “Assembly of Exogenous Fibronectin by Fibronectin-Null Cells is Dependent on the Adhesive Substrate,” J. Biol. Chem. 279(34):35749-35759 (2004) and Xu et al., “Display of Cell Surface Sites for Fibronectin Assembly is Modulated by Cell Adherence to (1)F3 and C-Terminal Modules of Fibronectin,” PLoS One 4(1):e4113 (2009), which are hereby incorporated by reference in their entirety). To assess the effects of fibronectin matrix mimetic substrates on the ability of cells to assemble a fibronectin matrix, immunofluorescence microscopy was used to visualize fibronectin fibril formation by FN-null MEFs, which assemble exogenous fibronectin into ECM fibrils by mechanisms similar to those of fibronectin-expressing cells (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111(19):2933-2943 (1998), which is hereby incorporated by reference in its entirety). α5β1 integrin-specific substrates (GST/III1H,8-10 and fibronectin) did not support the assembly of a fibrillar fibronectin matrix (FIG. 12). In contrast, matrix mimetic substrates that bind αvβ3 integrins (GST/III1H,8,10 and GST/III1H,8^(RGD)) supported fibronectin fibril formation (FIG. 12).

Fibronectin binding and deposition by FN-null MEFs adherent to matrix mimetic substrates was quantified by immunoblot analysis of cell/matrix lysates. Consistent with the immunofluorescence images shown in FIG. 12, fibronectin was absent from lysates of cells adherent to the α5β1 integrin-binding substrate, GST/III1H,8-10, but present in lysates from cells adherent to αvβ3-binding substrates (FIG. 13A). Interestingly, fibronectin deposition by cells adherent to the matrix mimetic substrate that binds solely via αvβ3 integrins (GST/III1H,8^(RGD)) was approximately two-fold greater than that of GST/III1H,8,10 (FIGS. 13A and 13B), which binds to cells through both αvβ3 and α5β1 integrins.

Fibronectin binding was also assessed by quantifying Alexa-labeled FN⁴⁸⁸ accumulation by cells adherent to the various matrix mimetics. Similar to results shown in FIG. 13A, fibronectin accumulation by cells adherent to the αvβ3-binding substrates, GST/III-1H,8,10 and GST/III1H, 8RGD, was significantly greater than that of cells adherent to GST/III1H,8-10 (FIG. 13C). In addition, the amount of fibronectin deposited by cells adherent to GST/III1H,8^(RGD) was approximately twice that of cells adherent to GST/III1H,8,10 (FIG. 13C). Fluorescence intensity of cell-free, FN⁴⁸⁸-treated wells was negligible for all substrates (FIG. 13C), indicating that FN⁴⁸⁸ does not bind directly to the matrix mimetics. Taken together, these data indicate that cells adherent to the αvβ3 integrin-specific substrate, GST/III1H,8^(RGD), incorporate significantly more fibronectin into a fibrillar matrix than GST/III1H,8,10, the α5β1 and αvβ3 integrin-binding substrate.

Example 9 ECM Collagen I Deposition by Cells Adherent to Fibronectin Matrix Mimetics

The deposition of collagen I into the ECM is dependent on the co-assembly of a fibronectin matrix (Sottile et al., “Fibronectin Polymerization Regulates the Composition and Stability of Extracellular Matrix Fibrils and Cell-Matrix Adhesions,” Mol. Biol. Cell. 13(10):3546-3559 (2002), which is hereby incorporated by reference in its entirety). To determine if the fibronectin matrix mimetics that support fibronectin matrix assembly also support collagen I deposition, FN-null MEFs adherent to saturating densities of matrix mimetics were incubated with FITC-labeled collagen I in the absence or presence of fibronectin. FITC-collagen I deposition was quantified 20 h after fibronectin and collagen addition. In the absence of fibronectin, FN-null MEFs adherent to the various matrix mimetics did not bind FITC-collagen I (FIG. 14A, ‘+cells, −FN’). Similarly, FITC-collagen I did not bind to the matrix mimetic substrates in the absence of cells (FIG. 14A, ‘−cells, −FN’), indicating that FITC-collagen I does not bind directly to the protein-coated plates. In the presence of soluble fibronectin, cells adherent to GST/III1H,8-10 showed limited collagen I deposition 20 h after treatment (FIG. 14A; ‘+cells, +FN’). In contrast, GST/III1H,8,10 and GST/III1H,8^(RGD) supported collagen I deposition by cells in the presence of fibronectin (FIG. 14A). GST/III1H,8^(RGD)-adherent cells treated with fibronectin showed a nearly two-fold increase in collagen I deposition compared to GST/III1H,8,10 (FIG. 14A), which was similar to the two-fold increase in fibronectin matrix deposition observed with GST/III1H,8^(RGD)-adherent cells (FIGS. 13B and 13C)

To determine if collagen I fibrils co-localized with fibronectin matrix fibrils, FITC-collagen I and fibronectin were visualized using immunofluorescence microscopy. FN-null MEFs adherent to GST/III1H,8,10 or GST/III1H,8^(RGD) displayed collagen fibrils that co-localized extensively with fibronectin fibrils (FIG. 14B). To determine whether the interaction of collagen with fibronectin was required for collagen deposition, FITC-collagen I and fibronectin were co-incubated in the presence of the R1R2 peptide, a protein fragment that inhibits fibronectin-collagen interactions without affecting fibronectin matrix assembly (Sottile et al., “Fibronectin-Dependent Collagen I Deposition Modulates the Cell Response to Fibronectin,” Am. J. Physiol. Cell Physiol. 293(6):C1934-1946 (2007), which is hereby incorporated by reference in its entirety). Addition of R1R2 blocked FITC-collagen I deposition by cells adherent to GST/III1H,8,10 and GST/III1H,8^(RGD) substrates (FIG. 14C). Co-incubation of fibronectin and FITC-collagen I with the control peptide, FNIII11C, had no effect on FITC-collagen I incorporation (FIG. 14C). These data indicate that fibronectin is required for collagen I deposition by cells adherent to fibronectin matrix mimetic substrates. Further, the αvβ3 integrin-binding substrate, GST/III1H,8^(RGD), supports increased fibronectin and collagen I deposition into the matrix compared to substrates that have an α5β1 integrin-binding component (GST/III1H,8-10 and GST/III1H,8,10).

Example 10 α5β1 Integrin Ligation and Translocation by Cells Adherent to Matrix Mimetic Substrates

Upon binding of soluble fibronectin to the cell surface, α5β1 integrins translocate centripetally from focal adhesions into mature matrix adhesions (Pankov et al., “Integrin Dynamics and Matrix Assembly: Tensin-Dependent Translocation of Alpha(5)Beta(1) Integrins Promotes Early Fibronectin Fibrillogenesis,” J. Cell Biol. 148(6):1075-1090 (2000), which is hereby incorporated by reference in its entirety). Integrin translocation along the actin cytoskeleton applies forces that unfold soluble fibronectin molecules to expose cryptic sites that allow for fibronectin multimerization and the establishment of an insoluble, fibrillar matrix (Zhong et al., “Rho-Mediated Contractility Exposes a Cryptic Site in Fibronectin and Induces Fibronectin Matrix Assembly,” J. Cell Biol. 141:539-551 (1998); Pankov et al., “Integrin Dynamics and Matrix Assembly: Tensin-Dependent Translocation of Alpha(5)Beta(1) Integrins Promotes Early Fibronectin Fibrillogenesis,” J. Cell Biol. 148(6):1075-1090 (2000); Danen et al., “The Fibronectin-Binding Integrins Alpha5beta1 and Alphavbeta3 Differentially Modulate RhoA-GTP Loading, Organization of Cell Matrix Adhesions, and Fibronectin Fibrillogenesis,” J. Cell Biol. 159(6):1071-1086 (2002); and Lemmon et al., “Cell Traction Forces Direct Fibronectin Matrix Assembly,” Biophys. J. 96(2):729-738 (2009), which are hereby incorporated by reference in their entirety). The data herein indicates the matrix mimetic substrate, GST/III1H,8-10, mediates cell adhesion through α5β1 integrins but does not support fibronectin matrix assembly. Thus, αvβ3 integrin-binding substrates (GST/III1H,8,10 and GST/III1H,8^(RGD)) may allow for a5β1 integrin translocation into matrix adhesions during the matrix assembly process, whereas on the GST/III1H,8-10 substrate, □α5β1 integrins remain in focal adhesions and matrix assembly is inhibited. To test this possibility, immunofluorescence microscopy was used to localize α5β1 integrins on cell surfaces following fibronectin fibril formation. FN-null MEFs were seeded onto plates pre-coated with saturating densities of the fibronectin matrix mimetics, then treated with soluble fibronectin for 20 h. α5β1 integrin-specific substrates (GST/III1H,8-10 and fibronectin) did not support cell-mediated assembly of a fibronectin matrix and had α5β1 integrin localized to central and peripheral focal adhesions (FIG. 15). In contrast, α5β1 integrins co-localized with fibronectin fibrils in matrix adhesions of cells adherent to GST/III1H,8,10 and GST/III1H,8^(RGD) (FIG. 15). These data indicate that α5β1 integrin translocation into fibrillar adhesions takes place only on substrates that ligate cells, at least in part, via αvβ3 integrins.

Example 11 Quantifying Substrate-Bound α5β1 Integrins

The preceding Examples indicate that saturating coating densities of GST/III1H,8,10 and GST/III1H,8^(RGD) support fibronectin matrix assembly and α5β1 integrin translocation, whereas GST/III1H,8-10 and full-length fibronectin do not support matrix assembly and retain α5β1 integrins in focal adhesions after fibronectin treatment. The preceding Examples therefore indicate that upon adhesion to GST/III1H,8-10, α5β1 integrins preferentially engage the adhesive substrate instead of soluble fibronectin, thus inhibiting the initiation of the matrix assembly process. To assess α5β1 integrin clustering in response to substrate adhesion, FN-null MEFs were allowed to adhere and spread for 4 h on plates pre-coated with saturating densities of matrix mimetics in the absence of soluble fibronectin. α5β1 integrins were visualized by immunofluorescence microscopy. As expected, α5β1 integrins co-localized with vinculin in central and peripheral focal adhesions of cells adherent to both GST/III1H,8-10 and full-length fibronectin (FIG. 16A). Cells adherent to GST/III1H,8,10, which lacks the α5β1 binding site in FNIII9, showed reduced α5β1 integrin clustering compared to GST/III1H,8-10, and α5β1 integrin-containing focal adhesions were localized primarily to the cell edge (FIG. 16A). α5β1 integrin staining was completely absent from cells adherent to GST/III1H,8^(RGD), despite strong vinculin staining of focal adhesions at the periphery of cells (FIG. 16A).

Substrate-bound α5β1 integrins were next quantified by treating adherent FN-null MEFs, in the absence of fibronectin, with a membrane-impermeable chemical cross-linker 4 h after seeding. In agreement with the immunofluorescence images shown in FIG. 16A, there was a significant increase in α5β1 integrins bound to the GST/III-1H,8-10 substrate versus GST/III1H,8,10 and GST/III1H,8^(RGD) substrates (FIG. 16B-16C). Interestingly, there were fewer α5β1 integrins bound to full-length fibronectin compared to that of GST/III1H,8-10 (FIG. 16B-16C). This may be due, in part, to the fact that despite coating fibronectin at a saturating density (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998), which is hereby incorporated by reference in its entirety), there is a 20-fold difference in the molar coating concentration compared to GST/III1H,8-10. Together, these data indicate that removal of FNIII9 from GST/III1H,8-10 reduces the amount of substrate-bound α5β1 integrins.

To determine if the total number of α5β1 integrin-binding sites in the mimetic substrate is a key regulator of fibronectin matrix assembly, FN-null MEFs were seeded on plates pre-coated with decreasing concentrations of GST/III1H,8-10 and substrate-bound integrins were isolated 4 h after seeding. There were no observable differences in the ability of cells to adhere and spread at any of the coating concentrations used. The amount of substrate-bound α5β1 integrin was significantly decreased when plates were coated with 25 nM and 50 nM GST/III1H,8-10 compared to 400 nM GST/III1H,8-10 (FIG. 17A-17B). These data indicate that the amount of α5β1 integrin engaged in the cell-substrate interactions is dependent on the coating density of GST/III1H,8-10.

Studies were conducted to determine whether decreasing the coating density of GST/III1H,8-10 and, thus, reducing α5β1 integrin-substrate ligation, would allow for cell-dependent fibronectin matrix assembly. FN-null MEFs adherent to wells coated with 25 nM GST/III1H,8-10 assembled a fibronectin matrix with α5β1 integrins in fibrillar adhesions (FIG. 17C), whereas cells adherent to plates coated with 400 nM GST/III1H,8-10 did not assemble fibronectin fibrils and retained α5β1 integrins in focal adhesions (FIG. 17C). Taken together, these data provide evidence that modulating the number of binding sites for α5β1 integrins in the adhesive substrate directly affects α5β1 integrin translocation and the assembly of a fibronectin matrix.

Example 12 Fibronectin Matrix Assembly and Cell Proliferation

The assembly of a fibronectin matrix stimulates cell proliferation (Sottile et al., “Fibronectin Matrix Assembly Enhances Adhesion-Dependent Cell Growth,” J. Cell Sci. 111:2933-2943 (1998), which is hereby incorporated by reference in its entirety). To determine whether the fibronectin matrix formed by FN-null cells adherent to the different fibronectin matrix mimetics similarly stimulates cell proliferation, FN-null MEFs adherent to the various fibronectin matrix mimetics were treated with soluble fibronectin and cell number was determined after 4 days. A protein coating concentration of 50 nM was used to allow for the assembly of a fibronectin matrix by cells adherent to GST/III-1H,8-10. Consistent with previous results, collagen-adherent FN-null MEFs displayed a 2.06-fold increase in cell number after 4 days with fibronectin treatment compared to cells treated with the vehicle control, PBS (FIG. 18A). Cells adherent to the α5β1 integrin-binding substrate, GST/III1H,8-10 displayed a 1.54-fold increase in cell number with fibronectin treatment over PBS-treated control (FIG. 18A). GST/III1H,8,10, the α5β1 and αvβ3 integrin-binding substrate, supported a 1.53-fold increase in cell number after 4 days with fibronectin treatment, while adhesion to the αvβ3 integrin-binding substrate, GST/III1H,8^(RGD), resulted in a 2.90-fold increase in cell number with fibronectin treatment over the vehicle control (FIG. 18A). At this coating concentration, there were no significant differences in the amount of FN⁴⁸⁸ deposited by cells adherent to GST/III1H,8-10, GST/III1H,8,10 or GST/III1H,8^(RGD) (FIG. 18B). Together, these data demonstrate that fibronectin matrix assembly stimulates proliferation of cells adherent to fibronectin matrix mimetics. Furthermore, compared to the α5β1 integrin-binding substrates (GST/III1H,8-10 and GST/III1H,8,10), the αvβ3 integrin-binding substrate (GST/III1H,8^(RGD)) supports the assembly of a more proliferative fibronectin matrix.

Example 13 FNIII1H,8,10 Promotes Wound Healing In Vivo

To test the effectiveness of the fibronectin peptide mimetics of the present invention to stimulate wound healing in vivo, GST/III1H,8,10 and GST/III1H,8^(RGD) mimetics were administered to wounds in a genetically-diabetic mouse model. Full thickness skin wounds were made on the dorsal side of C57BLKS/J-m+/+Lepr(db) mice (age 8-12 weeks) using a 6 mm biopsy punch (Miltex). Wounds were treated with either 15 μl of fibronectin matrix mimetics or GST (25 μM diluted in PBS) or PBS alone. Wounds were sealed from the environment with a 1 cm×1 cm piece of Tegaderm (3M Health Care). Mice were treated with mimetics, GST, or PBS immediately following surgery as well as on days 2, 4, 7, 9, 11, 14 and 16 after surgery with new Tegaderm being applied following each treatment. Fourteen days (n=3) or 18 days (n=1) after wounding, the animals were sacrificed and the skin surrounding the wound was excised (FIG. 19A, inset images) and embedded in paraffin. Four-micrometer sections were cut, mounted on slides, and stained for hematoxylin and eosin. Slides were viewed using an inverted microscope (Carl Zeiss MicroImaging) with a 5× objective. Images of the wound space were obtained with a digital camera (Model Infinity 2; Lumenera) and represent 1 of 4 experiments (FIG. 19A). Bar=200 μm. As shown in FIG. 19B, granulation tissue thickness in animals administered GST/III1H,8,10 and GST/III1H,8^(RGD) mimetics was significantly increased compared to animals administered PBS control. The granulation tissue thickness in animals administered GST/III1H,8,10 was also significantly increased compared to animals administered the GST control.

Although preferred embodiments have been depicted and described in detail herein, it will be apparent to those skilled in the relevant art that various modifications, additions, substitutions, and the like can be made without departing from the spirit of the invention and these are therefore considered to be within the scope of the invention as defined in the claims which follow. 

What is claimed:
 1. A wound healing composition comprising: a recombinant fibronectin peptide mimetic comprising: (i) at least a portion of the type III heparin-binding domain FNIII1H of fibronectin, wherein said portion comprises a heparin binding sequence and (ii) at least a portion of the type III integrin-binding domain FNIII8-10 of fibronectin, wherein said portion comprises an integrin binding sequence and does not contain FNIII9 in its entirety, wherein the at least a portion of the type III integrin binding domain comprises an amino acid sequence corresponding to amino acids 1266-1356 of SEQ ID NO:1 linked to amino acids 1447-1536 of SEQ ID NO: 1; and a synthetic material.
 2. The wound healing composition of claim 1, wherein the recombinant fibronectin peptide mimetic comprises the amino acid sequence of SEQ ID NO:
 3. 3. The wound healing composition of claim 1, wherein the synthetic material is selected from the group consisting of a biocompatible polymer, a biological dermal substitute, and a tissue scaffold.
 4. The wound healing composition of claim 3, wherein the synthetic material is a biocompatible polymer that is biostable, bioerodable, and/or bioresorbable.
 5. The wound healing composition of claim 4, wherein the biocompatible polymer comprises a biostable polymer selected from the group consisting of polyurethanes, isobutylene, polystyrene-isobutylene-polystyrene, silicone, a thermoplastic elastomer, an ethylene vinyl acetate copolymer, a polyolefin elastomer, EPDM ethylene-propylene terpolymer rubber, polyamide elastomer, hydrogel, and combinations thereof.
 6. The wound healing composition of claim 4, wherein the biocompatible polymer comprises a bioerodable or bioresorable polymer selected from the group consisting of polyglycolide, polylactide, poly(lactide-co-glycolide), polycaprolactone, polybutylene succinate, poly(p-dioxanone), polytrimethylene carbonate, polyphosphazenes, specific polyester polyurethanes, polyether polyurethanes, polyamides, polyorthoesters, polyester amides, maleic anhydride copolymers, poly(sebacic anhydride), polyvinyl alcohol, biopolymers, gelatin, glutens, cellulose, starches, chitin, chitosan, alginates, bacterial polymers, poly(hydroxybutyrate), poly(hydroxybutyrate-co-valerate), functionalized polymers, copolymers, and combinations or blends thereof.
 7. The wound healing composition of claim 3, wherein the biological dermal substitute is a collagen based dermal substitute.
 8. The wound healing composition of claim 3, wherein the tissue-scaffold is a three-dimensional tissue engineered organ.
 9. The wound healing composition of claim 1 further comprising: one or more additional recombinant proteins or peptides involved in wound healing.
 10. The wound healing composition of claim 9, wherein the one or more additional recombinant proteins or peptides is selected from the group consisting of extracellular matrix proteins, growth factors, cytokines, chemokines, and any combination thereof.
 11. The wound healing composition of claim 10, wherein the one or more additional recombinant proteins or peptides is an extracellular matrix protein selected from the group consisting of glycosaminoglycan, a proteoglycan, collagen, elastin, laminin, alginate, a chitin derivative, fibrin, fibrinogen, and any combination thereof.
 12. The wound healing composition of claim 10, wherein the one or more additional recombinant proteins or peptides is a growth factor selected from the group consisting of platelet derived growth factor (PDGF), tumor necrosis factor-alpha (TNF-α), TNF-β, epidermal growth factor (EGF), keratinocyte growth factor, vascular endothelial growth factors (VEGFs), fibroblast growth factors (FGFs), tumor necrosis factor, insulin growth factor (IGF), and any combination thereof.
 13. The wound healing composition of claim 9, wherein the one or more additional recombinant proteins or peptides are spatially patterned throughout the synthetic material.
 14. The wound healing composition of claim 1 further comprising: a wound healing agent selected from the group consisting of anti-inflammatory agents, antimicrobial agents, healing promoters, and combinations thereof.
 15. The wound healing composition of claim 1, wherein the composition is formulated as a cream, gel, or ointment.
 16. A method of treating a wound comprising: providing the wound healing composition of claim 1, and applying said wound healing composition to the wound under conditions suitable to promote healing of the wound.
 17. A wound dressing comprising: the wound healing composition of claim 1 and a wound dressing material.
 18. The wound dressing of claim 17, wherein the wound dressing material is selected from the group consisting of gauze, film, gel, hydrocolloid, alginate, hydrogel, polysaccharide paste, granules, and beads.
 19. A method of treating a wound comprising: providing the wound dressing of claim 17 and applying said wound dressing to the wound under conditions suitable to promote healing of the wound.
 20. The method of claim 19, wherein said wound healing composition comprises a biocompatible polymer and said applying comprises: contacting the composition with the wound and allowing the composition to polymerize over the wound. 